A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036716



Internal ID19125935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134478027..134849662hg38UCSC Ensembl
Innerchr11:134347921..134719556hg19UCSC Ensembl
Innerchr11:133853131..134224766hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38371636
hg19371636
hg18371636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1308n100
Supporting Variantsnssv3710777, nssv3513441
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036716
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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