A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736265



Internal ID20512212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1765957..1766020hg38UCSC Ensembl
chr20:1746603..1746666hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736265
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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