A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494307



Internal ID21151860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68241163..68267861hg38UCSC Ensembl
chr13:68815295..68841993hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3826699
hg1926699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494307
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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