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nsv471659

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97,147

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 803 SVs from 68 studies. See in: genome view    
Remapped(Score: Pass):41,650,014-41,747,160Question Mark
Overlapping variant regions from other studies: 457 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):46,287,856-46,454,477Question Mark
Overlapping variant regions from other studies: 4 SVs from 2 studies. See in: genome view    
Submitted genomic43,553,554-43,720,175Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv471659RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr941,650,01441,747,160
nsv471659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr946,287,85646,454,477
nsv471659Submitted genomicNCBI34 (hg16)Primary AssemblyGPC_000000201.1Chr943,553,55443,720,175

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv548937copy number lossGM10970BAC aCGHProbe signal intensity55
nssv548938copy number lossGM10976BAC aCGHProbe signal intensity56
nssv548939copy number lossGM10979BAC aCGHProbe signal intensity65
nssv548940copy number lossGM11523BAC aCGHProbe signal intensity54
nssv548941copy number lossGM15726BAC aCGHProbe signal intensity41
nssv548942copy number lossGM15727BAC aCGHProbe signal intensity44
nssv548943copy number lossGM15732BAC aCGHProbe signal intensity56
nssv548944copy number lossGM15733BAC aCGHProbe signal intensity51
nssv548945copy number lossGM16688BAC aCGHProbe signal intensity44
nssv548946copy number gainJK1058BBAC aCGHProbe signal intensity61
nssv550439copy number lossGM10970BAC aCGHProbe signal intensity55
nssv550440copy number lossGM10976BAC aCGHProbe signal intensity56
nssv550441copy number lossGM10979BAC aCGHProbe signal intensity65
nssv550442copy number lossGM15724BAC aCGHProbe signal intensity41
nssv550443copy number lossGM15727BAC aCGHProbe signal intensity44
nssv550444copy number lossGM16688BAC aCGHProbe signal intensity44
nssv550445copy number gainJK1058BBAC aCGHProbe signal intensity61

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv548937RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548938RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548939RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548940RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548941RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548942RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548943RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548944RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548945RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv548946RemappedPassNC_000009.12:g.(?_
41650014)_(4173608
5_?)dup
GRCh38.p12First PassNC_000009.12Chr941,650,01441,736,085
nssv550439RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550440RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550441RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550442RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550443RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550444RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)del
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550445RemappedPassNC_000009.12:g.(?_
41650014)_(4174716
0_?)dup
GRCh38.p12First PassNC_000009.12Chr941,650,01441,747,160
nssv550439RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550440RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550441RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550442RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550443RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550444RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)del
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv550445RemappedPerfectNC_000009.11:g.(?_
46287856)_(4645447
7_?)dup
GRCh37.p13First PassNC_000009.11Chr946,287,85646,454,477
nssv548937RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548938RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548939RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548940RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548941RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548942RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548943RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548944RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548945RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)del
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv548946RemappedPerfectNC_000009.11:g.(?_
46298864)_(4640539
3_?)dup
GRCh37.p13First PassNC_000009.11Chr946,298,86446,405,393
nssv550439Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550440Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550441Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550442Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550443Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550444Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv550445Submitted genomicGPC_000000201.1:g.
(?_43553554)_(4372
0175_?)dup
NCBI34 (hg16)GPC_000000201.1Chr943,553,55443,720,175
nssv548937Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548938Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548939Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548940Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548941Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548942Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548943Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548944Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548945Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)del
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091
nssv548946Submitted genomicGPC_000000201.1:g.
(?_43564562)_(4367
1091_?)dup
NCBI34 (hg16)GPC_000000201.1Chr943,564,56243,671,091

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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