A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746751



Internal ID20522765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45472555..45472628hg38UCSC Ensembl
chr20:44101195..44101268hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264602
Samples
Known GenesWFDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746751
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer