A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035450



Internal ID19124669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42878760..42949618hg38UCSC Ensembl
Innerchr11:42900310..42971168hg19UCSC Ensembl
Innerchr11:42856886..42927744hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3870859
hg1970859
hg1870859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n100
Supporting Variantsnssv3509712, nssv3521996
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035450
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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