A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741681



Internal ID20517658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20954222..20990568hg38UCSC Ensembl
chr5:20954331..20990677hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3836347
hg1936347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741681
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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