A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051820



Internal ID15558320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886431..29942984hg38UCSC Ensembl
Innerchr6:29854208..29910761hg19UCSC Ensembl
Innerchr6:29962187..30018740hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3856554
hg1956554
hg1856554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601277
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)nssv1051820
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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