A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494111



Internal ID21151664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28446412..28551495hg38UCSC Ensembl
chr14:28915618..29020701hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38105084
hg19105084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer