A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491985



Internal ID21149538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68208465..68211120hg38UCSC Ensembl
chr13:68782597..68785252hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382656
hg192656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491985
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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