A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493067



Internal ID21150620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23091302..23112816hg38UCSC Ensembl
chr14:23560511..23582025hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3821515
hg1921515
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181788
Samples
Known GenesACIN1, C14orf119
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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