A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018841



Internal ID18761374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101117129..101225018hg38UCSC Ensembl
Innerchr7:100760410..100868299hg19UCSC Ensembl
Innerchr7:100547130..100655019hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38107890
hg19107890
hg18107890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655299
Samples
Known GenesAP1S1, MIR4653, MOGAT3, NAT16, PLOD3, SERPINE1, VGF, ZNHIT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018841
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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