A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489567



Internal ID21147120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61459201..61467200hg38UCSC Ensembl
chr13:62033334..62041333hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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