A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052828



Internal ID18795359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67730549..67893696hg38UCSC Ensembl
Innerchr11:67498020..67661167hg19UCSC Ensembl
Innerchr11:67254596..67417743hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38163148
hg19163148
hg18163148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1217n100
Supporting Variantsnssv3710625
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052828
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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