A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098809



Internal ID22008042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88473675..88473675hg38UCSC Ensembl
chr13:89125930..89125930hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098809
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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