A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150190



Internal ID15878693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54519416..54645591hg38UCSC Ensembl
Innerchr19:55030599..55157042hg19UCSC Ensembl
Innerchr19:59722411..59848854hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38126176
hg19126444
hg18126444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580239
Supporting Variants
SamplesHGDP01242
Known GenesKIR3DX1, LILRA1, LILRA2, LILRB1, MIR8061
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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