A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438099



Internal ID216670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27691543..27702161hg38UCSC Ensembl
chr4:27693165..27703783hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810619
hg1910619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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