A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193536



Internal ID20760576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115848419..115860076hg38UCSC Ensembl
chr10:117607930..117619587hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811658
hg1911658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446027
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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