A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526685



Internal ID15107292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34928743..34959645hg38UCSC Ensembl
Innerchr17:33255762..33286664hg19UCSC Ensembl
Innerchr17:30279875..30310777hg18UCSC Ensembl
Innerchr17:30279875..30310777hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3830903
hg1930903
hg1830903
hg1730903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703018
Samples
Known GenesCCT6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526685
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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