A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459273



Internal ID21116826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8787501..8795800hg38UCSC Ensembl
chr12:8940097..8948396hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1391n223
Supporting Variantsnssv18187012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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