A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601463



Internal ID16388872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29942973..29946600hg38UCSC Ensembl
Innerchr6:29910750..29914377hg19UCSC Ensembl
Innerchr6:30018729..30022356hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383628
hg193628
hg183628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10366n54
Supporting Variantsnssv1052241
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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