A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519794



Internal ID15100401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32585709..32594595hg38UCSC Ensembl
Innerchr19:33076615..33085501hg19UCSC Ensembl
Innerchr19:37768455..37777341hg18UCSC Ensembl
Innerchr19:37768455..37777341hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg388887
hg198887
hg188887
hg178887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658735, nssv693903, nssv678219
Samples
Known GenesPDCD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519794
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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