A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947074



Internal ID22722575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47255238..47255533hg38UCSC Ensembl
chr19:47758495..47758790hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947074
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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