A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046072



Internal ID20613112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2746653..2752663hg38UCSC Ensembl
chr19:2746651..2752661hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386011
hg196011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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