A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697782



Internal ID15434434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47232327..47240133hg38UCSC Ensembl
Innerchr17:45309693..45317499hg19UCSC Ensembl
Innerchr17:42664692..42672498hg18UCSC Ensembl
Innerchr17:42664692..42672498hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg387807
hg197807
hg187807
hg177807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521092
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697782
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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