A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602666



Internal ID16390075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32587882..32592854hg38UCSC Ensembl
Innerchr6:32555659..32560631hg19UCSC Ensembl
Innerchr6:32663637..32668609hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384973
hg194973
hg184973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1056364, nssv1056363
Samples
Known GenesHLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602666
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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