A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694924



Internal ID15431576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:122755427..122770940hg38UCSC Ensembl
Innerchr6:123076572..123092085hg19UCSC Ensembl
Innerchr6:123118271..123133784hg18UCSC Ensembl
Innerchr6:123118271..123133784hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3815514
hg1915514
hg1815514
hg1715514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522150
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694924
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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