A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901490



Internal ID16195446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54258559hg38UCSC Ensembl
Innerchr19:54731679..54762408hg19UCSC Ensembl
Innerchr19:59423491..59454220hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3830755
hg1930730
hg1830730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580192
Supporting Variants
Samples
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901490
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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