A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061789



Internal ID18804320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54303818hg38UCSC Ensembl
Innerchr19:54730202..54815093hg19UCSC Ensembl
Innerchr19:59422014..59506905hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3877490
hg1984892
hg1884892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3654n100
Supporting Variantsnssv3573402
Samples
Known GenesLILRA3, 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)nsv1061789
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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