A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054452



Internal ID19143671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61998408..62108238hg38UCSC Ensembl
Innerchr11:61765880..61875710hg19UCSC Ensembl
Innerchr11:61522456..61632286hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38109831
hg19109831
hg18109831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213n100
Supporting Variantsnssv3504359, nssv3510973
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)nsv1054452
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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