A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602259



Internal ID16389668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32574998hg38UCSC Ensembl
Innerchr6:32458912..32542775hg19UCSC Ensembl
Innerchr6:32566890..32650753hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3883864
hg1983864
hg1883864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054834, nssv1054835, nssv1054833
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)nsv602259
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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