A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690923



Internal ID15427575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19228707..19245067hg38UCSC Ensembl
Innerchr6:19228938..19245298hg19UCSC Ensembl
Innerchr6:19336917..19353277hg18UCSC Ensembl
Innerchr6:19336917..19353277hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3816361
hg1916361
hg1816361
hg1716361
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520164
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690923
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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