A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985197



Internal ID20552237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93464426..93472705hg38UCSC Ensembl
chr10:95224183..95232462hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg388280
hg198280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443030
Supporting Variants
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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