A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526079



Internal ID15453372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62973910..63009712hg38UCSC Ensembl
Innerchr17:61051271..61087073hg19UCSC Ensembl
Innerchr17:58405003..58440805hg18UCSC Ensembl
Innerchr17:58405003..58440805hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3835803
hg1935803
hg1835803
hg1735803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702323
Samples
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526079
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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