A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693335



Internal ID15429987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78291626..78291927hg38UCSC Ensembl
Innerchr17:76287707..76288008hg19UCSC Ensembl
Innerchr17:73799302..73799603hg18UCSC Ensembl
Innerchr17:73799302..73799603hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38302
hg19302
hg18302
hg17302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516327
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693335
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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