nsv821612

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,831

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 444 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):79,618,279-79,621,109Question Mark
Overlapping variant regions from other studies: 444 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):77,378,279-77,381,109Question Mark
Overlapping variant regions from other studies: 344 SVs from 18 studies. See in: genome view    
Submitted genomic75,479,267-75,482,097Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821612RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000018.10Chr1879,618,27979,621,109
nsv821612RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000018.9Chr1877,378,27977,381,109
nsv821612Submitted genomicNCBI36 (hg18)NC_000018.8Chr1875,479,26775,482,097

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1420018duplicationNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1420018RemappedPerfectNC_000018.10:g.(?_
79618279)_(7962110
9_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000018.10Chr1879,618,27979,621,109
nssv1420018RemappedPerfectNC_000018.9:g.(?_7
7378279)_(77381109
_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000018.9Chr1877,378,27977,381,109
nssv1420018Submitted genomicNC_000018.8:g.(?_7
5479267)_(75482097
_?)dup
NCBI36 (hg18)NC_000018.8Chr1875,479,26775,482,097

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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