A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601457



Internal ID16388866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29942755..29942954hg38UCSC Ensembl
Innerchr6:29910532..29910731hg19UCSC Ensembl
Innerchr6:30018511..30018710hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38200
hg19200
hg18200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052233, nssv1052234
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601457
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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