A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476233



Internal ID21133786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69157531..69182539hg38UCSC Ensembl
chr13:69731663..69756671hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3825009
hg1925009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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