A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208633



Internal ID20775675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40492659..40635807hg38UCSC Ensembl
chr3:40534150..40677298hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38143149
hg19143149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365381
Supporting Variants
Samples
Known GenesZNF620, ZNF621
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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