A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985191



Internal ID20552231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93345446..93364154hg38UCSC Ensembl
chr10:95105203..95123911hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3818709
hg1918709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440461
Supporting Variants
Samples
Known GenesMYOF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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