A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505901



Internal ID282663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115362836..115377172hg38UCSC Ensembl
chr10:117122346..117136682hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3814337
hg1914337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039270
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505901
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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