A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046326



Internal ID20613366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36108517..36108568hg38UCSC Ensembl
chr19:36599419..36599470hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02907


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