A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462745



Internal ID21120298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85867128..85869093hg38UCSC Ensembl
chr12:86260906..86262871hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381966
hg191966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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