A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957088



Internal ID22732228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52498807..52499050hg38UCSC Ensembl
chr20:51115346..51115589hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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