A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207945



Internal ID20774985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122345397..122364628hg38UCSC Ensembl
chr3:122064244..122083475hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3819232
hg1919232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361636
Supporting Variants
Samples
Known GenesCCDC58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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