A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053522



Internal ID15906708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31560353..31576412hg38UCSC Ensembl
Innerchr6:31528130..31544189hg19UCSC Ensembl
Innerchr6:31636109..31652168hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3816060
hg1916060
hg1816060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601941
Supporting Variants
Samples
Known GenesLTA, TNF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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