A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602261



Internal ID16389670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32581498hg38UCSC Ensembl
Innerchr6:32458912..32549275hg19UCSC Ensembl
Innerchr6:32566890..32657253hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3890364
hg1990364
hg1890364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054837, nssv1054842, nssv1054843, nssv1054839, nssv1054840, nssv1054841, nssv1054838
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)nsv602261
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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