A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049034



Internal ID20616074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58077107..58083049hg38UCSC Ensembl
chr19:58588474..58594416hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385943
hg195943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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