A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455778



Internal ID21113331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104432587..104439322hg38UCSC Ensembl
chr12:104826365..104833100hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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