A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051291



Internal ID19140510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100932536..100943895hg38UCSC Ensembl
Innerchr11:100803267..100814626hg19UCSC Ensembl
Innerchr11:100308477..100319836hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3811360
hg1911360
hg1811360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266n100
Supporting Variantsnssv3513725
Samples
Known GenesARHGAP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051291
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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