A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481106



Internal ID21138659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97044905..97073343hg38UCSC Ensembl
chr13:97697159..97725597hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3828439
hg1928439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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