A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065918



Internal ID19155137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54214089..54249722hg38UCSC Ensembl
Innerchr19:54717958..54753580hg19UCSC Ensembl
Innerchr19:59409770..59445392hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3835634
hg1935623
hg1835623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3655n100
Supporting Variantsnssv3573316, nssv3573317
Samples
Known GenesLILRA6, LILRB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065918
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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