A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463714



Internal ID241608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103637381..103654000hg38UCSC Ensembl
chr4:104558538..104575157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3816620
hg1916620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954339
Samples
Known GenesTACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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