A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695951



Internal ID15432603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135668512..135717089hg38UCSC Ensembl
Innerchr6:135989650..136038227hg19UCSC Ensembl
Innerchr6:136031343..136079920hg18UCSC Ensembl
Innerchr6:136031343..136079920hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3848578
hg1948578
hg1848578
hg1748578
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518511
Supporting Variants
Samples
Known GenesLINC00271, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695951
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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