A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580192



Internal ID16367601
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901488, nssv901491, nssv901489, nssv1150187, nssv901490
SamplesHGDP00206
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580192
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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