A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050751



Internal ID19139970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:135002410..135074876hg38UCSC Ensembl
Innerchr11:134872304..134944770hg19UCSC Ensembl
Innerchr11:134377514..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3872467
hg1972467
hg1872469
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1321n100
Supporting Variantsnssv3504777, nssv3710798, nssv3517072
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050751
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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