A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655808



Internal ID15045774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34377544..34384130hg38UCSC Ensembl
Innerchr17:32704563..32711149hg19UCSC Ensembl
Innerchr17:29728676..29735262hg18UCSC Ensembl
Innerchr17:29728676..29735262hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386587
hg196587
hg186587
hg176587
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517423
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655808
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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