A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089963



Internal ID21999196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18211710..18211710hg38UCSC Ensembl
chrUn_gl000212:40462..40462hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089963
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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