A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602786



Internal ID16390195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32661580..32666554hg38UCSC Ensembl
Innerchr6:32629357..32634331hg19UCSC Ensembl
Innerchr6:32737335..32742309hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384975
hg194975
hg184975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10600n54
Supporting Variantsnssv1056878, nssv1056879, nssv1056881, nssv1056882, nssv1056880
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602786
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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