A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098761



Internal ID21467436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60140761..60140761hg38UCSC Ensembl
chr15:60432960..60432960hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651355
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098761
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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