A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065887



Internal ID19155106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54518252..54641325hg38UCSC Ensembl
Innerchr19:55029435..55152776hg19UCSC Ensembl
Innerchr19:59721247..59844588hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38123074
hg19123342
hg18123342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573422
Samples
Known GenesKIR3DX1, LILRA1, LILRA2, LILRB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065887
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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