A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694113



Internal ID15430765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77568058..77651453hg38UCSC Ensembl
Innerchr6:78277775..78361170hg19UCSC Ensembl
Innerchr6:78334494..78417889hg18UCSC Ensembl
Innerchr6:78334494..78417889hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3883396
hg1983396
hg1883396
hg1783396
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521951
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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