A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579901



Internal ID16020624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48033582..48046691hg38UCSC Ensembl
Innerchr19:48536839..48549948hg19UCSC Ensembl
Innerchr19:53228651..53241760hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3813110
hg1913110
hg1813110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899987
Samples
Known GenesCABP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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