A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601831



Internal ID16389240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31356440..31359946hg38UCSC Ensembl
Innerchr6:31324217..31327723hg19UCSC Ensembl
Innerchr6:31432196..31435702hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383507
hg193507
hg183507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10442n54
Supporting Variantsnssv1053307
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601831
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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