A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037830



Internal ID19127049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100931790..100947398hg38UCSC Ensembl
Innerchr11:100802521..100818129hg19UCSC Ensembl
Innerchr11:100307731..100323339hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3815609
hg1915609
hg1815609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1267n100
Supporting Variantsnssv3504334
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)nsv1037830
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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