A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501420



Internal ID20874653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103944079..104113005hg38UCSC Ensembl
chr14:104410416..104579342hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38168927
hg19168927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186271
Samples
Known GenesASPG, TDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501420
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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