A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901440



Internal ID16195396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225208..54240257hg38UCSC Ensembl
Innerchr19:54729079..54744133hg19UCSC Ensembl
Innerchr19:59420891..59435945hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815050
hg1915055
hg1815055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580171
Supporting Variants
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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