A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045037



Internal ID19134256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134877688..134987472hg38UCSC Ensembl
Innerchr11:134747582..134857366hg19UCSC Ensembl
Innerchr11:134252792..134362576hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38109785
hg19109785
hg18109785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1316n100
Supporting Variantsnssv3710794
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)nsv1045037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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