A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039558



Internal ID18782089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:534242..672091hg38UCSC Ensembl
Innerchr11:534242..672091hg19UCSC Ensembl
Innerchr11:524242..662091hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38137850
hg19137850
hg18137850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506049
Samples
Known GenesC11orf35, CDHR5, DEAF1, DRD4, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039558
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