A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048522



Internal ID20615562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57000159..57000714hg38UCSC Ensembl
chr19:57511527..57512082hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048522
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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