A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601262



Internal ID16041985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29950980hg38UCSC Ensembl
Innerchr6:29851443..29918757hg19UCSC Ensembl
Innerchr6:29959422..30026736hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3867315
hg1967315
hg1867315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10347n54
Supporting Variantsnssv1051798
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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