A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708522



Internal ID15655792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1204036..1207482hg38UCSC Ensembl
Innerchr1:1139416..1142862hg19UCSC Ensembl
Innerchr1:1129279..1132725hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383447
hg193447
hg183447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544960
Supporting Variants
Samples
Known GenesTNFRSF18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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