A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545440



Internal ID15986163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12184201..12188908hg38UCSC Ensembl
Innerchr1:12244258..12248965hg19UCSC Ensembl
Innerchr1:12166845..12171552hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384708
hg194708
hg184708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113n54
Supporting Variantsnssv710020
Samples
Known GenesTNFRSF1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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