A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601460



Internal ID16388869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29942954..29945360hg38UCSC Ensembl
Innerchr6:29910731..29913137hg19UCSC Ensembl
Innerchr6:30018710..30021116hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg382407
hg192407
hg182407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10365n54
Supporting Variantsnssv1052237
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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