A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043841



Internal ID18786372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49725016..49948413hg38UCSC Ensembl
Innerchr11:49746568..49969965hg19UCSC Ensembl
Innerchr11:49703144..49926541hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38223398
hg19223398
hg18223398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1130n100
Supporting Variantsnssv3507394
Samples
Known GenesLOC440040
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043841
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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