A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405470



Internal ID184814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78194154..78194205hg38UCSC Ensembl
chr11:77905200..77905251hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048600
Samples
Known GenesUSP35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405470
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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