A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985223



Internal ID20552264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93785720..93786738hg38UCSC Ensembl
chr10:95545477..95546495hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439894
Supporting Variants
Samples
Known GenesLGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.8163


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