A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602182



Internal ID16389591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32597007hg38UCSC Ensembl
Innerchr6:32455482..32564784hg19UCSC Ensembl
Innerchr6:32563460..32672762hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38109303
hg19109303
hg18109303
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10504n54
Supporting Variantsnssv1054512, nssv1054513, nssv1054510, nssv1054507, nssv1054508, nssv1054509, nssv1054511
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602182
Frequency
Sample Size17421
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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