A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746698



Internal ID20522712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32176394..32177098hg38UCSC Ensembl
chr20:30764197..30764901hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746698
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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