A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083790



Internal ID21490685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88596178..88596178hg38UCSC Ensembl
chr15:89139409..89139409hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649865
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083790
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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