A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044015



Internal ID19133234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116382452..116415213hg38UCSC Ensembl
Innerchr11:116253169..116285930hg19UCSC Ensembl
Innerchr11:115758379..115791140hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832762
hg1932762
hg1832762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1282n100
Supporting Variantsnssv3512690
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)nsv1044015
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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