A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089656



Internal ID21483201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49832728..49832728hg38UCSC Ensembl
chr15:50124925..50124925hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655114
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089656
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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