A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469909



Internal ID247684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75331117..75331175hg38UCSC Ensembl
chr5:74626942..74627000hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469909
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