A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066892



Internal ID18809423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54236847..54340836hg38UCSC Ensembl
Innerchr19:54740723..54852107hg19UCSC Ensembl
Innerchr19:59432535..59543919hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38103990
hg19111385
hg18111385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3726563
Samples
Known GenesLILRA3, LILRA4, 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)nsv1066892
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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