A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061223



Internal ID18803754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54320705hg38UCSC Ensembl
Innerchr19:54730202..54831977hg19UCSC Ensembl
Innerchr19:59422014..59523789hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3894377
hg19101776
hg18101776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3573405, nssv3573404
Samples
Known GenesLILRA3, LILRA5, LILRA6, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061223
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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