A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698587



Internal ID122253
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 StatusS
Merged Variantsnsv5559608
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698587
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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