A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925593



Internal ID22700820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60615449..60647010hg38UCSC Ensembl
chr11:60382922..60414483hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3831562
hg1931562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363148
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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