A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147230



Internal ID346412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35699146..35707563hg38UCSC Ensembl
chr11:35720694..35729111hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388418
hg198418
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv71n206
Supporting Variantsnssv17044247
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147230
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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