A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743495



Internal ID20519483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58350435..58350714hg38UCSC Ensembl
chr20:56925491..56925770hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273875
Samples
Known GenesRAB22A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743495
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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