A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099777



Internal ID20666817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179484684..179488663hg38UCSC Ensembl
chr3:179202472..179206451hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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