A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963859



Internal ID22738795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52008853..52013667hg38UCSC Ensembl
chr20:50625392..50630206hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384815
hg194815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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