A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651316



Internal ID21599621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85395634..85395634hg38UCSC Ensembl
chr13:85969769..85969769hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096094
SamplesNA19239
Known GenesLINC00351
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651316
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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