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nsv442085

  • Variant Calls:24
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,770

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 273 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):102,711,399-102,718,168Question Mark
Overlapping variant regions from other studies: 273 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):102,351,846-102,358,615Question Mark
Overlapping variant regions from other studies: 8 SVs from 4 studies. See in: genome view    
Submitted genomic101,945,797-101,952,566Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv442085RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7102,711,399102,718,168
nsv442085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7102,351,846102,358,615
nsv442085Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr7101,945,797101,952,566

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv1634087copy number lossNA07034SNP arrayProbe signal intensity1143
nssv1634088copy number lossNA10861SNP arrayProbe signal intensity1161
nssv1634089copy number lossNA18506SNP arrayProbe signal intensity1190
nssv1634090copy number lossNA18508SNP arrayProbe signal intensity1192
nssv1634091copy number lossNA18592SNP arrayProbe signal intensity1153
nssv1634092copy number lossNA18853SNP arrayProbe signal intensity1172
nssv1634093copy number lossNA18859SNP arrayProbe signal intensity1166
nssv1634094copy number lossNA18860SNP arrayProbe signal intensity1167
nssv1634095copy number lossNA18861SNP arrayProbe signal intensity1171
nssv1634096copy number lossNA18870SNP arrayProbe signal intensity1192
nssv1634097copy number lossNA18872SNP arrayProbe signal intensity1180
nssv1634098copy number lossNA19116SNP arrayProbe signal intensity1177
nssv1634099copy number lossNA19120SNP arrayProbe signal intensity1179
nssv1634100copy number lossNA19138SNP arrayProbe signal intensity1154
nssv1634101copy number lossNA19140SNP arrayProbe signal intensity1182
nssv1634102copy number lossNA19143SNP arrayProbe signal intensity1183
nssv1634103copy number lossNA19193SNP arrayProbe signal intensity0180
nssv1634104copy number lossNA19194SNP arrayProbe signal intensity1176
nssv1634105copy number lossNA19200SNP arrayProbe signal intensity1184
nssv1634106copy number lossNA19206SNP arrayProbe signal intensity1185
nssv1634107copy number lossNA19209SNP arrayProbe signal intensity1190
nssv1634108copy number lossNA19211SNP arrayProbe signal intensity1169
nssv1634109copy number lossNA19221SNP arrayProbe signal intensity1185
nssv1634110copy number lossNA19222SNP arrayProbe signal intensity1182

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1634087RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634088RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634089RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634090RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634091RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634092RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634093RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634094RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634095RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634096RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634097RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634098RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634099RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634100RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634101RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634102RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634103RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634104RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634105RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634106RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634107RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634108RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634109RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634110RemappedPerfectNC_000007.14:g.(?_
102711399)_(102718
168_?)del
GRCh38.p12First PassNC_000007.14Chr7102,711,399102,718,168
nssv1634087RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634088RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634089RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634090RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634091RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634092RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634093RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634094RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634095RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634096RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634097RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634098RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634099RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634100RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634101RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634102RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634103RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634104RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634105RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634106RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634107RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634108RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634109RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634110RemappedPerfectNC_000007.13:g.(?_
102351846)_(102358
615_?)del
GRCh37.p13First PassNC_000007.13Chr7102,351,846102,358,615
nssv1634087Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634088Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634089Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634090Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634091Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634092Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634093Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634094Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634095Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634096Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634097Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634098Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634099Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634100Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634101Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634102Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634103Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634104Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634105Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634106Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634107Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634108Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634109Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566
nssv1634110Submitted genomicNC_000007.11:g.(?_
101945797)_(101952
566_?)del
NCBI35 (hg17)NC_000007.11Chr7101,945,797101,952,566

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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