A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901498



Internal ID15848768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54229182..54334531hg38UCSC Ensembl
Innerchr19:54733056..54845802hg19UCSC Ensembl
Innerchr19:59424868..59537614hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38105350
hg19112747
hg18112747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580198
Supporting Variants
Samples
Known GenesLILRA3, LILRA4, 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)nssv901498
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer