A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282079



Internal ID20491297
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 StatusS
Merged Variantsnsv4744122
Supporting Variants
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282079
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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