A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452427



Internal ID21109980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12295116..12345920hg38UCSC Ensembl
chr10:12337115..12387919hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3850805
hg1950805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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