A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601497



Internal ID16388906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269347..31270332hg38UCSC Ensembl
Innerchr6:31237124..31238109hg19UCSC Ensembl
Innerchr6:31345103..31346088hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38986
hg19986
hg18986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10374n54
Supporting Variantsnssv1052295
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601497
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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