A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459838



Internal ID21117391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87907636..87912851hg38UCSC Ensembl
chr12:88301413..88306628hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg385216
hg195216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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