A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951319



Internal ID22726684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23140060..23144418hg38UCSC Ensembl
chr20:23120697..23125055hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384359
hg194359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951319
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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