A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901495



Internal ID15848765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54333355hg38UCSC Ensembl
Innerchr19:54731679..54844626hg19UCSC Ensembl
Innerchr19:59423491..59536438hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38105551
hg19112948
hg18112948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580195
Supporting Variants
Samples
Known GenesLILRA3, LILRA5, LILRA6, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901495
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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