A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582058



Internal ID21530566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24076495..24076811hg38UCSC Ensembl
chr1:24402985..24403301hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063635
SamplesHG00731
Known GenesMYOM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582058
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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