A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704582



Internal ID15094548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10284612..10291344hg38UCSC Ensembl
Innerchr17:10187929..10194661hg19UCSC Ensembl
Innerchr17:10128654..10135386hg18UCSC Ensembl
Innerchr17:10128654..10135386hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386733
hg196733
hg186733
hg176733
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520771
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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