A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602400



Internal ID16389809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32517715..32551228hg38UCSC Ensembl
Innerchr6:32485492..32519005hg19UCSC Ensembl
Innerchr6:32593470..32626983hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3833514
hg1933514
hg1833514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10526n54
Supporting Variantsnssv1055385
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602400
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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