A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208671



Internal ID20775713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43663635..43683175hg38UCSC Ensembl
chr3:43705127..43724667hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3819541
hg1919541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364024
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125


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