A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997569



Internal ID21906912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53676008..53677577hg38UCSC Ensembl
chr4:54542175..54543744hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997569
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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