A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051829



Internal ID15558329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888127..29942954hg38UCSC Ensembl
Innerchr6:29855904..29910731hg19UCSC Ensembl
Innerchr6:29963883..30018710hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3854828
hg1954828
hg1854828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601284
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)nssv1051829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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