A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207982



Internal ID20775022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160225401..160227500hg38UCSC Ensembl
chr3:159943188..159945287hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361438
Supporting Variants
Samples
Known GenesC3orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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