A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080199



Internal ID21452016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67946725..67946725hg38UCSC Ensembl
chr15:68239063..68239063hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382085
hg192085
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653928
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080199
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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