A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191486



Internal ID20758526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115226197..115253374hg38UCSC Ensembl
chr10:116985989..117012844hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3827178
hg1926856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442548
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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