A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518619



Internal ID20891980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33178513..33183387hg38UCSC Ensembl
chr19:33669419..33674293hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384875
hg194875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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