A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609082



Internal ID16396491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154168113..154248437hg38UCSC Ensembl
Innerchr7:153865198..153945522hg19UCSC Ensembl
Innerchr7:153496131..153576455hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3880325
hg1980325
hg1880325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099690
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609082
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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