A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051139



Internal ID19140358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100931790..100948716hg38UCSC Ensembl
Innerchr11:100802521..100819447hg19UCSC Ensembl
Innerchr11:100307731..100324657hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3816927
hg1916927
hg1816927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1267n100
Supporting Variantsnssv3513592
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)nsv1051139
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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