A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977473



Internal ID20544513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115757209..115763954hg38UCSC Ensembl
chr10:117516720..117523465hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386746
hg196746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447158
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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