A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559608



Internal ID332637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25847457..25848457hg38UCSC Ensembl
chr15:26092604..26093604hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698587
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559608
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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