A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694613



Internal ID15084579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33406743..33593135hg38UCSC Ensembl
Innerchr17:31733761..31920154hg19UCSC Ensembl
Innerchr17:28757874..28944267hg18UCSC Ensembl
Innerchr17:28757874..28944267hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38186393
hg19186394
hg18186394
hg17186394
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521841
Supporting Variants
Samples
Known GenesAA06, ASIC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694613
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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