A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660559



Internal ID21608864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25829338..25829338hg38UCSC Ensembl
chr15:26074485..26074485hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095471
SamplesHG03065
Known GenesATP10A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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