A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486037



Internal ID21143590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82336801..82359800hg38UCSC Ensembl
chr13:82910936..82933935hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3823000
hg1923000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1935n223
Supporting Variantsnssv18184835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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