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nsv428268

  • Variant Calls:18
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,181

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 377 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):169,812,865-169,916,045Question Mark
Overlapping variant regions from other studies: 380 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):169,782,006-169,885,186Question Mark
Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
Submitted genomic168,048,630-168,151,810Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv428268RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1169,812,865169,916,045
nsv428268RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1169,782,006169,885,186
nsv428268Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1168,048,630168,151,810

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv452341copy number lossHGDP00449BAC aCGHProbe signal intensity126
nssv452354copy number gainHGDP00450BAC aCGHProbe signal intensity88
nssv452365copy number gainHGDP00462BAC aCGHProbe signal intensity83
nssv452376copy number lossHGDP00463BAC aCGHProbe signal intensity90
nssv452387copy number gainHGDP00471BAC aCGHProbe signal intensity73
nssv452398copy number lossHGDP00472BAC aCGHProbe signal intensity65
nssv452409copy number lossHGDP00476BAC aCGHProbe signal intensity69
nssv452420copy number lossHGDP00984BAC aCGHProbe signal intensity75
nssv452431copy number lossHGDP01086BAC aCGHProbe signal intensity52
nssv452442copy number lossHGDP01088BAC aCGHProbe signal intensity78
nssv452453copy number lossHGDP01089BAC aCGHProbe signal intensity65
nssv452465copy number lossHGDP01093BAC aCGHProbe signal intensity95
nssv452476copy number lossNA18498BAC aCGHProbe signal intensity97
nssv452487copy number lossNA19096BAC aCGHProbe signal intensity100
nssv452498copy number lossNA19113BAC aCGHProbe signal intensity122
nssv452509copy number lossNA19147BAC aCGHProbe signal intensity75
nssv452520copy number lossNA19181BAC aCGHProbe signal intensity87
nssv452531copy number lossNA19225BAC aCGHProbe signal intensity71

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv452341RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452354RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)dup
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452365RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)dup
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452376RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452387RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)dup
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452398RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452409RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452420RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452431RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452442RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452453RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452465RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452476RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452487RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452498RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452509RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452520RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452531RemappedPerfectNC_000001.11:g.(?_
169812865)_(169916
045_?)del
GRCh38.p12First PassNC_000001.11Chr1169,812,865169,916,045
nssv452341RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452354RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)dup
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452365RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)dup
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452376RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452387RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)dup
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452398RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452409RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452420RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452431RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452442RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452453RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452465RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452476RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452487RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452498RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452509RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452520RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452531RemappedPerfectNC_000001.10:g.(?_
169782006)_(169885
186_?)del
GRCh37.p13First PassNC_000001.10Chr1169,782,006169,885,186
nssv452341Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452354Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)dup
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452365Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)dup
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452376Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452387Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)dup
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452398Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452409Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452420Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452431Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452442Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452453Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452465Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452476Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452487Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452498Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452509Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452520Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810
nssv452531Submitted genomicNC_000001.9:g.(?_1
68048630)_(1681518
10_?)del
NCBI36 (hg18)NC_000001.9Chr1168,048,630168,151,810

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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