A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154293



Internal ID15880501
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
SamplesNINDS_22
Known GenesLTA, TNF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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