A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602265



Internal ID16389674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32582601hg38UCSC Ensembl
Innerchr6:32458912..32550378hg19UCSC Ensembl
Innerchr6:32566890..32658356hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891467
hg1991467
hg1891467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054858, nssv1054857
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)nsv602265
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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