A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468907



Internal ID246699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117619209..117647593hg38UCSC Ensembl
chr5:116954904..116983288hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828385
hg1928385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468907
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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