A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491455



Internal ID21149008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54394201..54399300hg38UCSC Ensembl
chr14:54860919..54866018hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187213
Samples
Known GenesCDKN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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