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nsv471620

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:150,673

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 531 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):84,831,663-84,982,335Question Mark
Overlapping variant regions from other studies: 252 SVs from 39 studies. See in: genome view    
Remapped(Score: Good):31,696-175,849Question Mark
Overlapping variant regions from other studies: 531 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):84,880,814-85,031,486Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic84,801,715-84,952,387Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv471620RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,831,66384,982,335
nsv471620RemappedGoodGRCh38.p12PATCHESSecond PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nsv471620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr384,880,81485,031,486
nsv471620Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000003.8Chr384,801,71584,952,387

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv550754copy number lossGM10469ABAC aCGHProbe signal intensity56
nssv550755copy number lossGM10471BAC aCGHProbe signal intensity51
nssv550756copy number lossGM10473ABAC aCGHProbe signal intensity44
nssv550757copy number lossGM10492ABAC aCGHProbe signal intensity47
nssv550758copy number lossGM10494ABAC aCGHProbe signal intensity55
nssv550759copy number lossGM10496ABAC aCGHProbe signal intensity59
nssv550760copy number lossGM15726BAC aCGHProbe signal intensity41
nssv550761copy number lossJK1051ABAC aCGHProbe signal intensity53
nssv550762copy number lossJK1058BBAC aCGHProbe signal intensity61
nssv550763copy number lossJK1061BAC aCGHProbe signal intensity51
nssv550764copy number lossJK1688BBAC aCGHProbe signal intensity53
nssv550765copy number lossJK776BAC aCGHProbe signal intensity50
nssv550766copy number lossP86GABAC aCGHProbe signal intensity50

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv550754RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550755RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550756RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550757RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550758RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550759RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550760RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550761RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550762RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550763RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550764RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550765RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550766RemappedGoodNW_018654711.1:g.(
?_31696)_(175849_?
)del
GRCh38.p12Second PassNW_018654711.1Chr3|NW_01
8654711.1
31,696175,849
nssv550754RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550755RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550756RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550757RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550758RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550759RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550760RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550761RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550762RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550763RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550764RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550765RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550766RemappedPerfectNC_000003.12:g.(?_
84831663)_(8498233
5_?)del
GRCh38.p12First PassNC_000003.12Chr384,831,66384,982,335
nssv550754RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550755RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550756RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550757RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550758RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550759RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550760RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550761RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550762RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550763RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550764RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550765RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550766RemappedPerfectNC_000003.11:g.(?_
84880814)_(8503148
6_?)del
GRCh37.p13First PassNC_000003.11Chr384,880,81485,031,486
nssv550754Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550755Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550756Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550757Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550758Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550759Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550760Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550761Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550762Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550763Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550764Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550765Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387
nssv550766Submitted genomicNC_000003.8:g.(?_8
4801715)_(84952387
_?)del
NCBI34 (hg16)NC_000003.8Chr384,801,71584,952,387

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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