A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601834



Internal ID16389243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31356693..31357717hg38UCSC Ensembl
Innerchr6:31324470..31325494hg19UCSC Ensembl
Innerchr6:31432449..31433473hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381025
hg191025
hg181025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10443n54
Supporting Variantsnssv1053310
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601834
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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