A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142582



Internal ID341783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35098000..35106000hg38UCSC Ensembl
chr9:35097997..35105997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021537
Samples
Known GenesFAM214B, STOML2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142582
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