A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699996



Internal ID15436648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64298631..64351719hg38UCSC Ensembl
Innerchr6:65008524..65061612hg19UCSC Ensembl
Innerchr6:65066483..65119571hg18UCSC Ensembl
Innerchr6:65066483..65119571hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3853089
hg1953089
hg1853089
hg1753089
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524118
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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