A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450698



Internal ID21108251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93332401..93336500hg38UCSC Ensembl
chr10:95092158..95096257hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985190
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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