A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208628



Internal ID20775670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164696432..164724380hg38UCSC Ensembl
chr3:164414220..164442168hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3827949
hg1927949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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