A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489865



Internal ID21147418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125955841..125972434hg38UCSC Ensembl
chr12:126440387..126456980hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3816594
hg1916594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193717
Samples
Known GenesLINC00939
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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