A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462620



Internal ID240546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121365550..121365673hg38UCSC Ensembl
chr4:122286705..122286828hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954557
Samples
Known GenesQRFPR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462620
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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