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nsv893093

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,184

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 324 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):39,149,212-39,258,395Question Mark
Overlapping variant regions from other studies: 480 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):39,149,209-39,258,392Question Mark
Overlapping variant regions from other studies: 264 SVs from 25 studies. See in: genome view    
Submitted genomic39,139,209-39,248,392Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv893093RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr939,149,21239,157,13639,235,72939,258,395
nsv893093RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr939,149,20939,157,13339,235,72639,258,392
nsv893093Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr939,139,20939,147,13339,225,72639,248,392

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1547428copy number gainMS17373SNP arraySNP genotyping analysis17
nssv1551078copy number lossMS18756SNP arraySNP genotyping analysis18

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1547428RemappedPerfectNC_000009.12:g.(39
149212_39157136)_(
39235729_39258395)
dup		GRCh38.p12First PassNC_000009.12Chr939,149,21239,157,13639,235,72939,258,395
nssv1551078RemappedPerfectNC_000009.12:g.(39
149212_39157136)_(
39235729_39258395)
del		GRCh38.p12First PassNC_000009.12Chr939,149,21239,157,13639,235,72939,258,395
nssv1547428RemappedPerfectNC_000009.11:g.(39
149209_39157133)_(
39235726_39258392)
dup		GRCh37.p13First PassNC_000009.11Chr939,149,20939,157,13339,235,72639,258,392
nssv1551078RemappedPerfectNC_000009.11:g.(39
149209_39157133)_(
39235726_39258392)
del		GRCh37.p13First PassNC_000009.11Chr939,149,20939,157,13339,235,72639,258,392
nssv1547428Submitted genomicNC_000009.10:g.(39
139209_39147133)_(
39225726_39248392)
dup		NCBI36 (hg18)NC_000009.10Chr939,139,20939,147,13339,225,72639,248,392
nssv1551078Submitted genomicNC_000009.10:g.(39
139209_39147133)_(
39225726_39248392)
del		NCBI36 (hg18)NC_000009.10Chr939,139,20939,147,13339,225,72639,248,392

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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