A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093962



Internal ID21478514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85681719..85681719hg38UCSC Ensembl
chr15:86224950..86224950hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649508
Supporting Variants
SamplesHG03486
Known GenesAKAP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093962
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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