A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698999



Internal ID15088965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36084845..36092731hg38UCSC Ensembl
Innerchr17:34412202..34420079hg19UCSC Ensembl
Innerchr17:31436315..31444192hg18UCSC Ensembl
Innerchr17:31436315..31444192hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387887
hg197878
hg187878
hg177878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523265
Supporting Variants
Samples
Known GenesCCL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698999
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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