A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040848



Internal ID21950186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32377235..32377340hg38UCSC Ensembl
chr20:30965038..30965143hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620807
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040848
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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