A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096097



Internal ID20663137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153798221..153800353hg38UCSC Ensembl
chr3:153516010..153518142hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096097
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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