A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495332



Internal ID21152885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80544427..80594720hg38UCSC Ensembl
chr14:81010771..81061064hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3850294
hg1950294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178148
Samples
Known GenesCEP128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495332
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