A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118155



Internal ID21301421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:80844070..80919433hg38UCSC Ensembl
InnerchrX:80099569..80174932hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3875364
hg1975364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1270n145
Supporting Variantsnssv14104052
Samplessample24
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118155
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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