A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141848



Internal ID341047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35052000..35112000hg38UCSC Ensembl
chr9:35051997..35111997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3860001
hg1960001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021535
Samples
Known GenesFAM214B, FANCG, PIGO, STOML2, VCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141848
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