A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085024



Internal ID21486458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85513776..85515966hg38UCSC Ensembl
chr15:86057007..86059197hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587458
Supporting Variants
SamplesNA12878
Known GenesAKAP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085024
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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