A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496714



Internal ID20869917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103590610..103591917hg38UCSC Ensembl
chr14:104056947..104058254hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188494
Samples
Known GenesAPOPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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