A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155620



Internal ID22086125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54518264..54641337hg38UCSC Ensembl
Outerchr19:54515214..54645888hg38UCSC Ensembl
Innerchr19:55029447..55152788hg19UCSC Ensembl
Outerchr19:55026398..55157337hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38130675
hg19130940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013717, nssv4013718
Samples
Known GenesKIR3DX1, LILRA1, LILRA2, LILRB1, MIR8061
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155620
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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