A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697580



Internal ID15434232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22036638..22043580hg38UCSC Ensembl
Innerchr6:22036867..22043809hg19UCSC Ensembl
Innerchr6:22144846..22151788hg18UCSC Ensembl
Innerchr6:22144846..22151788hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386943
hg196943
hg186943
hg176943
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520732
Supporting Variants
Samples
Known GenesCASC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697580
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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