A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038734



Internal ID18781265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132954183..133396436hg38UCSC Ensembl
Innerchr11:132824078..133266331hg19UCSC Ensembl
Innerchr11:132329288..132771541hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38442254
hg19442254
hg18442254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n100
Supporting Variantsnssv3710769, nssv3512273, nssv3514934, nssv3518213
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038734
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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