A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093914



Internal ID20660954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138920026..138922017hg38UCSC Ensembl
chr3:138638868..138640859hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381992
hg191992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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