A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207851



Internal ID20774891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112550701..112582100hg38UCSC Ensembl
chr3:112269548..112300947hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3831400
hg1931400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372784
Supporting Variants
Samples
Known GenesATG3, SLC35A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00107


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