A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209727



Internal ID20776768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15338081..15339451hg38UCSC Ensembl
chr3:15379588..15380958hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367824
Supporting Variants
Samples
Known GenesSH3BP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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