A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743790



Internal ID20519780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34653856..34656286hg38UCSC Ensembl
chr20:33241660..33244090hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262749
Samples
Known GenesPIGU
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743790
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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