A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579108



Internal ID16366517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24389817..24448802hg38UCSC Ensembl
Innerchr19:24572619..24631604hg19UCSC Ensembl
Innerchr19:24364459..24423444hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3858986
hg1958986
hg1858986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897016
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579108
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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