A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733694



Internal ID20509624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63888690..63888772hg38UCSC Ensembl
chr20:62520043..62520125hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290635
Samples
Known GenesTPD52L2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733694
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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