A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053098



Internal ID15906284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31317933..31355013hg38UCSC Ensembl
Innerchr6:31285710..31322790hg19UCSC Ensembl
Innerchr6:31393689..31430769hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837081
hg1937081
hg1837081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601725
Supporting Variants
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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