A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695257



Internal ID15431909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80819622..80897666hg38UCSC Ensembl
Innerchr6:81529339..81607383hg19UCSC Ensembl
Innerchr6:81586058..81664102hg18UCSC Ensembl
Innerchr6:81586058..81664102hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3878045
hg1978045
hg1878045
hg1778045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517853
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695257
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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