A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606252



Internal ID16393661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13236436..13276626hg38UCSC Ensembl
Innerchr7:13276061..13316251hg19UCSC Ensembl
Innerchr7:13242586..13282776hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3840191
hg1940191
hg1840191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155298
SamplesHGDP01217
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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