A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931770



Internal ID22707059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33393160..33393265hg38UCSC Ensembl
chr19:33884066..33884171hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406578
Samples
Known GenesPEPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931770
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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