A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093292



Internal ID20660332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13761112..13772588hg38UCSC Ensembl
chr3:13802609..13814085hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3811477
hg1911477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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