A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509595



Internal ID286244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59180164..59180223hg38UCSC Ensembl
chr11:58947637..58947696hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047090
Samples
Known GenesDTX4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509595
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