A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479946



Internal ID21137499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109912679..109924337hg38UCSC Ensembl
chr12:110350484..110362142hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3811659
hg1911659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182797
Samples
Known GenesTCHP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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