A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460696



Internal ID238668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161113661..161123315hg38UCSC Ensembl
chr5:160540668..160550322hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg389655
hg199655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460696
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