A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602524



Internal ID16389933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554310..32658151hg38UCSC Ensembl
Innerchr6:32522087..32625928hg19UCSC Ensembl
Innerchr6:32630065..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38103842
hg19103842
hg18103842
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10554n54
Supporting Variantsnssv1055766, nssv1055763, nssv1055767, nssv1055762, nssv1055765, nssv1055764
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602524
Frequency
Sample Size17421
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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