A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479181



Internal ID21136734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111613462..111645347hg38UCSC Ensembl
chr12:112051266..112083151hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3831886
hg1931886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183733
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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