A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114805



Internal ID21298071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69841418..69845609hg38UCSC Ensembl
Innerchr9:72456334..72460525hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg384192
hg194192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1237n145
Supporting Variantsnssv14088056, nssv14089611, nssv14088096, nssv14090865
Samplessample313, sample329, sample101, sample216
Known GenesC9orf135
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114805
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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