A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495117



Internal ID21152670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85109080..85111229hg38UCSC Ensembl
chr13:85683215..85685364hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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