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nsv3169883

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,366

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 778 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):97,735,251-97,763,616Question Mark
Overlapping variant regions from other studies: 778 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):97,070,955-97,099,320Question Mark
Overlapping variant regions from other studies: 286 SVs from 24 studies. See in: genome view    
Submitted genomic97,096,711-97,125,076Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv3169883RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr597,735,25197,736,83697,758,03097,763,616
nsv3169883RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr597,070,95597,072,54097,093,73497,099,320
nsv3169883Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr597,096,71197,098,29697,119,49097,125,076

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv14248327deletionPML_2SNP arraySNP genotyping analysis1148
nssv14248966duplicationNGO_8SNP arraySNP genotyping analysis3119

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv14248327RemappedPerfectNC_000005.10:g.(97
735251_97736832)_(
97758030_97763616)
del		GRCh38.p12First PassNC_000005.10Chr597,735,25197,736,83297,758,03097,763,616
nssv14248966RemappedPerfectNC_000005.10:g.(97
735251_97736832)_(
97758030_97763616)
dup		GRCh38.p12First PassNC_000005.10Chr597,735,25197,736,83297,758,03097,763,616
nssv14248327RemappedPerfectNC_000005.9:g.(970
70955_97072536)_(9
7093734_97099320)d
el		GRCh37.p13First PassNC_000005.9Chr597,070,95597,072,53697,093,73497,099,320
nssv14248966RemappedPerfectNC_000005.9:g.(970
70955_97072536)_(9
7093734_97099320)d
up		GRCh37.p13First PassNC_000005.9Chr597,070,95597,072,53697,093,73497,099,320
nssv14248327Submitted genomicNC_000005.8:g.(970
96711_97098292)_(9
7119490_97125076)d
el		NCBI36 (hg18)NC_000005.8Chr597,096,71197,098,29297,119,49097,125,076
nssv14248966Submitted genomicNC_000005.8:g.(970
96711_97098292)_(9
7119490_97125076)d
up		NCBI36 (hg18)NC_000005.8Chr597,096,71197,098,29297,119,49097,125,076

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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