A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139447



Internal ID338632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142100553..142368436hg38UCSC Ensembl
chr3:141819395..142087278hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38267884
hg19267884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940997
Samples
Known GenesGK5, TFDP2, XRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139447
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