A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514910



Internal ID20888265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86957209..86957866hg38UCSC Ensembl
chr15:87500440..87501097hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027861
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514910
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