A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469252



Internal ID247041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68895810..68898894hg38UCSC Ensembl
chr5:68191637..68194721hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469252
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer