A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697601



Internal ID15087567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20281188..20619131hg38UCSC Ensembl
Innerchr17:20184501..20522444hg19UCSC Ensembl
Innerchr17:20125093..20463036hg18UCSC Ensembl
Innerchr17:20125093..20463036hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38337944
hg19337944
hg18337944
hg17337944
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520772
Supporting Variants
Samples
Known GenesCCDC144CP, CDRT15L2, KRT16P3, LGALS9B, SPECC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697601
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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