A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602657



Internal ID16390066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32582477..32658151hg38UCSC Ensembl
Innerchr6:32550254..32625928hg19UCSC Ensembl
Innerchr6:32658232..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3875675
hg1975675
hg1875675
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10554n54
Supporting Variantsnssv1056336, nssv1056335
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)nsv602657
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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