A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604767



Internal ID16392176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140380286..140494971hg38UCSC Ensembl
Innerchr6:140701423..140816108hg19UCSC Ensembl
Innerchr6:140743116..140857801hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38114686
hg19114686
hg18114686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073802
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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