A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702247



Internal ID15438899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79889517..79897744hg38UCSC Ensembl
Innerchr17:77863316..77871543hg19UCSC Ensembl
Innerchr17:75477911..75486138hg18UCSC Ensembl
Innerchr17:75477911..75486138hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388228
hg198228
hg188228
hg178228
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526017
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702247
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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