A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491255



Internal ID21148808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121668280..121674309hg38UCSC Ensembl
chr12:122106186..122112215hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg386030
hg196030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191566
Samples
Known GenesMORN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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