A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093322



Internal ID20660362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108589001..108589900hg38UCSC Ensembl
chr3:108307848..108308747hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367639
Supporting Variants
Samples
Known GenesDZIP3, KIAA1524
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00181


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