A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488836



Internal ID21146389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64974237..64983143hg38UCSC Ensembl
chr14:65440955..65449861hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg388907
hg198907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194028
Samples
Known GenesCHURC1-FNTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488836
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