A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038119



Internal ID18780650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17723368..17773030hg38UCSC Ensembl
Innerchr11:17744915..17794577hg19UCSC Ensembl
Innerchr11:17701491..17751153hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3849663
hg1949663
hg1849663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505677
Samples
Known GenesKCNC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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