A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059726



Internal ID18802257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54330126hg38UCSC Ensembl
Innerchr19:54730202..54841398hg19UCSC Ensembl
Innerchr19:59422014..59533210hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38103798
hg19111197
hg18111197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3660n100
Supporting Variantsnssv3573406
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)nsv1059726
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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