A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463418



Internal ID21120971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21846980..21847957hg38UCSC Ensembl
chr12:21999914..22000891hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192378
Samples
Known GenesABCC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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