A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472349



Internal ID22530241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83013657..83016156hg38UCSC Ensembl
chr15:83682409..83684908hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472349
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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