A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507413



Internal ID22565361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54132374..54137900hg38UCSC Ensembl
chr8:55044934..55050460hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg385527
hg195527
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853914
Supporting Variants
Samples
Known GenesMRPL15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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