A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744122



Internal ID20520118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32376873..32377009hg38UCSC Ensembl
chr20:30964676..30964812hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282079
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744122
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