A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545436



Internal ID15986159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12069994..12081404hg38UCSC Ensembl
Innerchr1:12130051..12141461hg19UCSC Ensembl
Innerchr1:12052638..12064048hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3811411
hg1911411
hg1811411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173674
Samples1780862021_A
Known GenesTNFRSF8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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