A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144829



Internal ID344034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95646378..95666002hg38UCSC Ensembl
chr14:96112715..96132339hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3819625
hg1919625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698650
Samples
Known GenesTCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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