A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085981



Internal ID21502754
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 Variantsnsv5600301
Supporting Variants
SamplesNA19239
Known GenesMYEF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085981
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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