A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545437



Internal ID15986160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12180767..12184201hg38UCSC Ensembl
Innerchr1:12240824..12244258hg19UCSC Ensembl
Innerchr1:12163411..12166845hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383435
hg193435
hg183435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710015
Samples
Known GenesTNFRSF1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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