A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699406



Internal ID15089372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10117373..10118325hg38UCSC Ensembl
Innerchr17:10020690..10021642hg19UCSC Ensembl
Innerchr17:9961415..9962367hg18UCSC Ensembl
Innerchr17:9961415..9962367hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38953
hg19953
hg18953
hg17953
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520771
Supporting Variants
Samples
Known GenesGAS7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699406
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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