A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951896



Internal ID22727237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62294456..62295273hg38UCSC Ensembl
chr20:60869512..60870329hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409045
Samples
Known GenesOSBPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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