A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602511



Internal ID16389920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553010..32553420hg38UCSC Ensembl
Innerchr6:32520787..32521197hg19UCSC Ensembl
Innerchr6:32628765..32629175hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38411
hg19411
hg18411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055720
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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