A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150179



Internal ID15876066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54195523..54245159hg38UCSC Ensembl
Innerchr19:54699386..54749011hg19UCSC Ensembl
Innerchr19:59391198..59440823hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3849637
hg1949626
hg1849626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580148
Supporting Variants
SamplesHGDP00780
Known GenesLILRA6, LILRB3, RPS9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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