A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462365



Internal ID21119918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130097551..130101948hg38UCSC Ensembl
chr11:129967446..129971843hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384398
hg194398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987770
Samples
Known GenesAPLP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462365
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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