A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094565



Internal ID20661605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119700949..119701497hg38UCSC Ensembl
chr3:119419796..119420344hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.14584


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