A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948547



Internal ID22724023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38651624..38651836hg38UCSC Ensembl
chr20:37280267..37280479hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948547
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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