A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602644



Internal ID16390053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32581949..32658151hg38UCSC Ensembl
Innerchr6:32549726..32625928hg19UCSC Ensembl
Innerchr6:32657704..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3876203
hg1976203
hg1876203
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10554n54
Supporting Variantsnssv1056304, nssv1056305, nssv1056303, nssv1056306
Samples
Known GenesHLA-DQA1, HLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602644
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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