A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737759



Internal ID20513722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10802681..10802741hg38UCSC Ensembl
chr20:10783329..10783389hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737759
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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