A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994596



Internal ID21903939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107721701..107721752hg38UCSC Ensembl
chr4:108642857..108642908hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994596
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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