A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941731



Internal ID22717160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14252339..14490204hg38UCSC Ensembl
chr20:14232985..14470850hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38237866
hg19237866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396159
Samples
Known GenesFLRT3, MACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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