A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087380



Internal ID21459374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85843399..85843648hg38UCSC Ensembl
chr15:86386630..86386879hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584986
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087380
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