A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710755



Internal ID19009036
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 StatusS
Merged Variantsnsv1040918
Supporting Variants
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)nssv3710755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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