A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050386



Internal ID18792917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132954183..133393689hg38UCSC Ensembl
Innerchr11:132824078..133263584hg19UCSC Ensembl
Innerchr11:132329288..132768794hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38439507
hg19439507
hg18439507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n100
Supporting Variantsnssv3520834
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050386
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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