A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090684



Internal ID21464058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82255854..82256078hg38UCSC Ensembl
chr15:82548195..82548419hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593724
Supporting Variants
SamplesHG03065
Known GenesEFTUD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090684
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