A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492339



Internal ID21149892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41273305..41306361hg38UCSC Ensembl
chr13:41847441..41880497hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3833057
hg1933057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492339
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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