A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704643



Internal ID15094609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36843263..36861944hg38UCSC Ensembl
Innerchr17:35200527..35219205hg19UCSC Ensembl
Innerchr17:32274640..32293318hg18UCSC Ensembl
Innerchr17:32274640..32293318hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3818682
hg1918679
hg1818679
hg1718679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528102
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704643
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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