A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456152



Internal ID21113705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55900233..55900893hg38UCSC Ensembl
chr12:56294017..56294677hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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