A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601667



Internal ID16389076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31314218..31353908hg38UCSC Ensembl
Innerchr6:31281995..31321685hg19UCSC Ensembl
Innerchr6:31389974..31429664hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3839691
hg1939691
hg1839691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10379n54
Supporting Variantsnssv1053028
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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