A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966005



Internal ID22740940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53724369..53730566hg38UCSC Ensembl
chr20:52340908..52347105hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386198
hg196198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966005
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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