A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051822



Internal ID15558322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886431..29944617hg38UCSC Ensembl
Innerchr6:29854208..29912394hg19UCSC Ensembl
Innerchr6:29962187..30020373hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3858187
hg1958187
hg1858187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601278
Supporting Variants
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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