A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117141



Internal ID21300407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16309399..16359720hg38UCSC Ensembl
Innerchr7:16349024..16399345hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3850322
hg1950322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n145
Supporting Variantsnssv14083327
Samplessample86
Known GenesISPD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117141
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