A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496240



Internal ID20869440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89859617..89859988hg38UCSC Ensembl
chr15:90402849..90403220hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026905
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496240
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