A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457819



Internal ID235855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77638684..77654647hg38UCSC Ensembl
chr4:78559838..78575801hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3815964
hg1915964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457819
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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