A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665223



Internal ID15055189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34320812..34333130hg38UCSC Ensembl
Innerchr17:32647831..32660149hg19UCSC Ensembl
Innerchr17:29671944..29684262hg18UCSC Ensembl
Innerchr17:29671944..29684262hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812319
hg1912319
hg1812319
hg1712319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517423
Supporting Variants
Samples
Known GenesCCL8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665223
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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