A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698606



Internal ID15088572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10264999..10272037hg38UCSC Ensembl
Innerchr17:10168316..10175354hg19UCSC Ensembl
Innerchr17:10109041..10116079hg18UCSC Ensembl
Innerchr17:10109041..10116079hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
hg177039
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)nssv698606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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