A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485753



Internal ID21143306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52746075..52746836hg38UCSC Ensembl
chr14:53212793..53213554hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194947
Samples
Known GenesSTYX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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