A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511875



Internal ID288443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60683572..60684261hg38UCSC Ensembl
chr11:60451045..60451734hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047836
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511875
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