A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145888



Internal ID21486926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110390353..110390353hg38UCSC Ensembl
chr9:113152633..113152633hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641262
Supporting Variants
SamplesNA12878
Known GenesSVEP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145888
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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