A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208902



Internal ID20775942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103057420..103122280hg38UCSC Ensembl
chr3:102776264..102841124hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3864861
hg1964861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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