A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579112



Internal ID16366521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24412774..24448802hg38UCSC Ensembl
Innerchr19:24595576..24631604hg19UCSC Ensembl
Innerchr19:24387416..24423444hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3836029
hg1936029
hg1836029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897020
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579112
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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