A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651980



Internal ID15041946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33782230..34498242hg38UCSC Ensembl
Innerchr17:32109249..32825261hg19UCSC Ensembl
Innerchr17:29133362..29849374hg18UCSC Ensembl
Innerchr17:29133362..29849374hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38716013
hg19716013
hg18716013
hg17716013
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)nssv651980
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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