A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693520



Internal ID15430172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164867280..164930068hg38UCSC Ensembl
Innerchr6:165280769..165343557hg19UCSC Ensembl
Innerchr6:165200759..165263547hg18UCSC Ensembl
Innerchr6:165251180..165313968hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3862789
hg1962789
hg1862789
hg1762789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693520
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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