A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012943



Internal ID21922286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93469949..93470087hg38UCSC Ensembl
chr10:95229706..95229844hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587779
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012943
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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