A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143009



Internal ID342210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119058364..119114364hg38UCSC Ensembl
chr11:118929075..118985074hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3856001
hg1956000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052224
Samples
Known GenesC2CD2L, DPAGT1, H2AFX, HMBS, VPS11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143009
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