A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090762



Internal ID21512143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81010864..81010864hg38UCSC Ensembl
chr14:81477208..81477208hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660780
Supporting Variants
SamplesNA24385
Known GenesTSHR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090762
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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