A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142326



Internal ID341526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67601387..67633393hg38UCSC Ensembl
chr9:44747977..46291915hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3832007
hg191543939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024210
Samples
Known GenesFAM27A, FAM27C, FAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142326
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