A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577086



Internal ID16364495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62356049..62393930hg38UCSC Ensembl
Innerchr18:60023282..60061163hg19UCSC Ensembl
Innerchr18:58174262..58212143hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3837882
hg1937882
hg1837882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884983
Samples
Known GenesTNFRSF11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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