A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094899



Internal ID20661939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135919691..135920078hg38UCSC Ensembl
chr3:135638533..135638920hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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