A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463146



Internal ID21120699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:59224367..59347573hg38UCSC Ensembl
chr12:59618148..59741354hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38123207
hg19123207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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