A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658735



Internal ID15048701
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 StatusS
Merged Variantsnsv519794
Supporting Variants
Samples
Known GenesPDCD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658735
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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