A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580162



Internal ID16367571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54224752..54236829hg38UCSC Ensembl
Innerchr19:54728623..54740705hg19UCSC Ensembl
Innerchr19:59420435..59432517hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3812078
hg1912083
hg1812083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6551n54
Supporting Variantsnssv901415
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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