A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460851



Internal ID238821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76780563..76781322hg38UCSC Ensembl
chr4:77701716..77702475hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952375
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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