A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150180



Internal ID15872807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54205409..54239341hg38UCSC Ensembl
Innerchr19:54709277..54743217hg19UCSC Ensembl
Innerchr19:59401089..59435029hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3833933
hg1933941
hg1833941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580150
Supporting Variants
SamplesHGDP00045
Known GenesLILRA6, LILRB3, RPS9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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