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nsv469706

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156,818

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 376 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):78,655,013-78,811,830Question Mark
Overlapping variant regions from other studies: 376 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):80,414,770-80,571,587Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic79,759,373-79,916,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1078,655,01378,811,830
nsv469706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1080,414,77080,571,587
nsv469706Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000010.7Chr1079,759,37379,916,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1672064copy number lossBAC aCGHProbe signal intensity
nssv1672083copy number lossBAC aCGHProbe signal intensity
nssv1672271copy number lossBAC aCGHProbe signal intensity
nssv1672537copy number lossBAC aCGHProbe signal intensity
nssv1672837copy number lossBAC aCGHProbe signal intensity
nssv1673387copy number lossBAC aCGHProbe signal intensity
nssv1673593copy number lossBAC aCGHProbe signal intensity
nssv1674294copy number lossBAC aCGHProbe signal intensity
nssv1675017copy number lossBAC aCGHProbe signal intensity
nssv1675027copy number lossBAC aCGHProbe signal intensity
nssv1675133copy number lossBAC aCGHProbe signal intensity
nssv1675143copy number lossBAC aCGHProbe signal intensity
nssv1675874copy number lossBAC aCGHProbe signal intensity
nssv1676447copy number lossBAC aCGHProbe signal intensity
nssv1676572copy number lossBAC aCGHProbe signal intensity
nssv1676580copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1672064RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1672083RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1672271RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1672537RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1672837RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1673387RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1673593RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1674294RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1675017RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1675027RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1675133RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1675143RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1675874RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1676447RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1676572RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1676580RemappedPerfectNC_000010.11:g.(?_
78655013)_(7881183
0_?)del
GRCh38.p12First PassNC_000010.11Chr1078,655,01378,811,830
nssv1672064RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1672083RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1672271RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1672537RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1672837RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1673387RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1673593RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1674294RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1675017RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1675027RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1675133RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1675143RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1675874RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1676447RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1676572RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1676580RemappedPerfectNC_000010.10:g.(?_
80414770)_(8057158
7_?)del
GRCh37.p13First PassNC_000010.10Chr1080,414,77080,571,587
nssv1672064Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1672083Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1672271Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1672537Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1672837Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1673387Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1673593Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1674294Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1675017Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1675027Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1675133Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1675143Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1675874Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1676447Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1676572Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190
nssv1676580Submitted genomicNC_000010.7:g.(?_7
9759373)_(79916190
_?)del
NCBI34 (hg16)NC_000010.7Chr1079,759,37379,916,190

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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