A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580242



Internal ID16367651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54637036..54675793hg38UCSC Ensembl
Innerchr19:55148487..55187279hg19UCSC Ensembl
Innerchr19:59840299..59879091hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3838758
hg1938793
hg1838793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901638
Samples
Known GenesLILRB1, LILRB4, MIR8061
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580242
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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