A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040918



Internal ID19130137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117328875..117354603hg38UCSC Ensembl
Innerchr11:117199591..117225319hg19UCSC Ensembl
Innerchr11:116704801..116730529hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3825729
hg1925729
hg1825729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710755
Samples
Known GenesCEP164
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040918
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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