A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602176



Internal ID16389585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32574357hg38UCSC Ensembl
Innerchr6:32455482..32542134hg19UCSC Ensembl
Innerchr6:32563460..32650112hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3886653
hg1986653
hg1886653
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10504n54
Supporting Variantsnssv1054478, nssv1054486, nssv1054484, nssv1054480, nssv1054477, nssv1054483, nssv1054481, nssv1054476, nssv1054482, nssv1054485, nssv1054479, nssv1054475, nssv1054474
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602176
Frequency
Sample Size17421
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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