A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997984



Internal ID21907327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52465415..52466051hg38UCSC Ensembl
chr4:53331581..53332217hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997984
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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