A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046499



Internal ID20613539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45463253..45465906hg38UCSC Ensembl
chr19:45966511..45969164hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382654
hg192654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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