A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698123



Internal ID15434775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33500374..33512961hg38UCSC Ensembl
Innerchr6:33468151..33480738hg19UCSC Ensembl
Innerchr6:33576129..33588716hg18UCSC Ensembl
Innerchr6:33576129..33588716hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812588
hg1912588
hg1812588
hg1712588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521506
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698123
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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