A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579299



Internal ID16366708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31238200..31271998hg38UCSC Ensembl
Innerchr19:31729106..31762904hg19UCSC Ensembl
Innerchr19:36420946..36454744hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3833799
hg1933799
hg1833799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898293
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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