A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155619



Internal ID22086124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54237443hg38UCSC Ensembl
Outerchr19:54218406..54249482hg38UCSC Ensembl
Innerchr19:54730202..54741319hg19UCSC Ensembl
Outerchr19:54722275..54753340hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3831077
hg1931066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv162n97
Supporting Variantsnssv4013713, nssv4013708, nssv4013710, nssv4013714, nssv4013712, nssv4013716, nssv4013715, nssv4013709, nssv4013711
Samples
Known GenesLILRA6, LILRB3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155619
Frequency
Sample Size131
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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