A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365688



Internal ID22591357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93426890..93428195hg38UCSC Ensembl
chr10:95186647..95187952hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912947
Supporting Variants
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365688
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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