A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601828



Internal ID16389237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31354736..31355406hg38UCSC Ensembl
Innerchr6:31322513..31323183hg19UCSC Ensembl
Innerchr6:31430492..31431162hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38671
hg19671
hg18671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053304
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601828
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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