A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602472



Internal ID16389881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32536102..32572264hg38UCSC Ensembl
Innerchr6:32503879..32540041hg19UCSC Ensembl
Innerchr6:32611857..32648019hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3836163
hg1936163
hg1836163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10543n54
Supporting Variantsnssv1055667
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602472
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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