A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640474



Internal ID21588779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110373614..110373614hg38UCSC Ensembl
chr9:113135894..113135894hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151175
SamplesHG03065
Known GenesSVEP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640474
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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