A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091125



Internal ID21469841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39779261..39779261hg38UCSC Ensembl
chr15:40071462..40071462hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651606
Supporting Variants
SamplesHG03125
Known GenesFSIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091125
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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