A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460589



Internal ID238567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84624346..84625898hg38UCSC Ensembl
chr4:85545499..85547051hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381553
hg191553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953614
Samples
Known GenesCDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460589
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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