A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518059



Internal ID20891420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29624823..29632992hg38UCSC Ensembl
chr19:30115730..30123899hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388170
hg198170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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