A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602407



Internal ID16389816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32519533..32526013hg38UCSC Ensembl
Innerchr6:32487310..32493790hg19UCSC Ensembl
Innerchr6:32595288..32601768hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386481
hg196481
hg186481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10527n54
Supporting Variantsnssv1055418, nssv1055417
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602407
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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