A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946957



Internal ID22722457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4464674..4468882hg38UCSC Ensembl
chr20:4445321..4449529hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384209
hg194209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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