A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207915



Internal ID20774955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119621100..119636591hg38UCSC Ensembl
chr3:119339947..119355438hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3815492
hg1915492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356670
Supporting Variants
Samples
Known GenesPLA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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