A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601608



Internal ID16389017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31312324..31422007hg38UCSC Ensembl
Innerchr6:31280101..31389784hg19UCSC Ensembl
Innerchr6:31388080..31497763hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38109684
hg19109684
hg18109684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1052771
Samples
Known GenesHLA-B, MICA, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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