A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602561



Internal ID16389970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32557911..32568104hg38UCSC Ensembl
Innerchr6:32525688..32535881hg19UCSC Ensembl
Innerchr6:32633666..32643859hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3810194
hg1910194
hg1810194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055892
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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