A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607802



Internal ID16395211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93361809..93387119hg38UCSC Ensembl
Innerchr7:92991121..93016431hg19UCSC Ensembl
Innerchr7:92829057..92854367hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825311
hg1925311
hg1825311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1090181
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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