A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084727



Internal ID21490831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89765654..89765654hg38UCSC Ensembl
chr15:90308885..90308885hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650690
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084727
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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