A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090555



Internal ID20657595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102633159..102633691hg38UCSC Ensembl
chr3:102352003..102352535hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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