A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489363



Internal ID21146916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89300589..89361096hg38UCSC Ensembl
chr13:89952843..90013350hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3860508
hg1960508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489363
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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