A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449436



Internal ID21106989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115281087..115284392hg38UCSC Ensembl
chr10:117040597..117043902hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383306
hg193306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977936
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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