A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150189



Internal ID15877259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54519000..54641641hg38UCSC Ensembl
Innerchr19:55030183..55153092hg19UCSC Ensembl
Innerchr19:59721995..59844904hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38122642
hg19122910
hg18122910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580238
Supporting Variants
SamplesHGDP00957
Known GenesKIR3DX1, LILRA1, LILRA2, LILRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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