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nsv515145

  • Variant Calls:20
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,970

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1004 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):590,578-608,547Question Mark
Overlapping variant regions from other studies: 1006 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):590,578-608,547Question Mark
Overlapping variant regions from other studies: 483 SVs from 27 studies. See in: genome view    
Submitted genomic580,578-598,547Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv515145RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9590,578608,547
nsv515145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9590,578608,547
nsv515145Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr9580,578598,547

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv2974369copy number lossNA18862Oligo aCGHProbe signal intensity0485
nssv2974370copy number lossNA18863Oligo aCGHProbe signal intensity1474
nssv2974371copy number lossNA18873Oligo aCGHProbe signal intensity1433
nssv2974372copy number lossNA18875Oligo aCGHProbe signal intensity1443
nssv2974373copy number lossNA18933Oligo aCGHProbe signal intensity1448
nssv2974374copy number lossNA19102Oligo aCGHProbe signal intensity1454
nssv2974375copy number lossNA19108Oligo aCGHProbe signal intensity1451
nssv2974376copy number lossNA19109Oligo aCGHProbe signal intensity1451
nssv2974377copy number lossNA19149Oligo aCGHProbe signal intensity1447
nssv2974378copy number lossNA19159Oligo aCGHProbe signal intensity1449
nssv2974379copy number lossNA19198Oligo aCGHProbe signal intensity1488
nssv2974380copy number lossNA19201Oligo aCGHProbe signal intensity1463
nssv2974381copy number lossNA19202Oligo aCGHProbe signal intensity1466
nssv2974382copy number lossNA19210Oligo aCGHProbe signal intensity1485
nssv2974383copy number lossNA19211Oligo aCGHProbe signal intensity1481
nssv2974384copy number lossNA19235Oligo aCGHProbe signal intensity1458
nssv2974385copy number lossNA19248Oligo aCGHProbe signal intensity1482
nssv2974386copy number lossNA19249Oligo aCGHProbe signal intensity1487
nssv2974387copy number lossNA21600Oligo aCGHProbe signal intensity1437
nssv2974388copy number lossNA21601Oligo aCGHProbe signal intensity1436

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv2974369RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974370RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974371RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974372RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974373RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974374RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974375RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974376RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974377RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974378RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974379RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974380RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974381RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974382RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974383RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974384RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974385RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974386RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974387RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974388RemappedPerfectNC_000009.12:g.(?_
590578)_(608547_?)
del
GRCh38.p12First PassNC_000009.12Chr9590,578608,547
nssv2974369RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974370RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974371RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974372RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974373RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974374RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974375RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974376RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974377RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974378RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974379RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974380RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974381RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974382RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974383RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974384RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974385RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974386RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974387RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974388RemappedPerfectNC_000009.11:g.(?_
590578)_(608547_?)
del
GRCh37.p13First PassNC_000009.11Chr9590,578608,547
nssv2974369Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974370Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974371Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974372Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974373Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974374Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974375Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974376Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974377Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974378Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974379Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974380Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974381Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974382Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974383Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974384Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974385Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974386Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974387Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547
nssv2974388Submitted genomicNC_000009.10:g.(?_
580578)_(598547_?)
del
NCBI36 (hg18)NC_000009.10Chr9580,578598,547

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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