A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467249



Internal ID245068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96506388..96582040hg38UCSC Ensembl
chr5:95842092..95917744hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3875653
hg1975653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467249
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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