A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464002



Internal ID241888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15821682..15824908hg38UCSC Ensembl
chr5:15821791..15825017hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962803
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464002
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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