A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208924



Internal ID20775964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105035268..105037684hg38UCSC Ensembl
chr3:104754112..104756528hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382417
hg192417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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