A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544961



Internal ID15985684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1205055..1211644hg38UCSC Ensembl
Innerchr1:1140435..1147024hg19UCSC Ensembl
Innerchr1:1130298..1136887hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg386590
hg196590
hg186590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv24n54
Supporting Variantsnssv708523
Samples
Known GenesTNFRSF18, TNFRSF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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