A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602823



Internal ID16043546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33086269..33086898hg38UCSC Ensembl
Innerchr6:33054046..33054675hg19UCSC Ensembl
Innerchr6:33162024..33162653hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38630
hg19630
hg18630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1057627, nssv1057636, nssv1057634, nssv1057628, nssv1057633, nssv1057631, nssv1057629, nssv1057630, nssv1057632, nssv1057635
Samples
Known GenesHLA-DPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602823
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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