A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602113



Internal ID16389522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32462952..32538126hg38UCSC Ensembl
Innerchr6:32430729..32505903hg19UCSC Ensembl
Innerchr6:32538707..32613881hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3875175
hg1975175
hg1875175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10487n54
Supporting Variantsnssv1053914
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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