A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411696



Internal ID191002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68478436..68478487hg38UCSC Ensembl
chr2:68705568..68705619hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915081
Samples
Known GenesAPLF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411696
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