A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371630



Internal ID22597299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48152993..48153043hg38UCSC Ensembl
chr15:48445190..48445240hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944228
Supporting Variants
Samples
Known GenesMYEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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