A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462809



Internal ID240731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100104528..100105261hg38UCSC Ensembl
chr4:101025685..101026418hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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