A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985194



Internal ID20552234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93426601..93428400hg38UCSC Ensembl
chr10:95186358..95188157hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447842
Supporting Variants
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00556


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