A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516976



Internal ID20890337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58440661..58444201hg38UCSC Ensembl
chr19:58952028..58955568hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383541
hg193541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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