A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388368



Internal ID22446238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64692128..64692245hg38UCSC Ensembl
chr15:64984327..64984444hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931284
Supporting Variants
Samples
Known GenesOAZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388368
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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