A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560202



Internal ID333215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41268831..41268832hg38UCSC Ensembl
chr15:41561029..41561030hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701109
Samples
Known GenesCHP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560202
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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