A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487434



Internal ID21144987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25029876..25030573hg38UCSC Ensembl
chr13:25604014..25604711hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487434
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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