A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679296



Internal ID15069262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33777656..34491743hg38UCSC Ensembl
Innerchr17:32104675..32818762hg19UCSC Ensembl
Innerchr17:29128788..29842875hg18UCSC Ensembl
Innerchr17:29128788..29842875hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38714088
hg19714088
hg18714088
hg17714088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517423
Supporting Variants
Samples
Known GenesASIC2, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679296
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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