A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708525



Internal ID15655795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1206945..1214281hg38UCSC Ensembl
Innerchr1:1142325..1149661hg19UCSC Ensembl
Innerchr1:1132188..1139524hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg387337
hg197337
hg187337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544963
Supporting Variants
Samples
Known GenesTNFRSF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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