A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087909



Internal ID21478692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417402..26417402hg38UCSC Ensembl
chr15:26662549..26662549hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652456
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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