A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040247



Internal ID19129466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116382452..116419204hg38UCSC Ensembl
Innerchr11:116253169..116289921hg19UCSC Ensembl
Innerchr11:115758379..115795131hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3836753
hg1936753
hg1836753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1282n100
Supporting Variantsnssv3710752
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)nsv1040247
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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