A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959454



Internal ID22734486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32372873..32373056hg38UCSC Ensembl
chr20:30960676..30960859hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391666
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959454
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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