A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492322



Internal ID21149875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112412506..112413732hg38UCSC Ensembl
chr12:112850310..112851536hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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