A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926456



Internal ID22701683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132239979..132240029hg38UCSC Ensembl
chr11:132109873..132109923hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350345
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926456
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