A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048893



Internal ID19138112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134841075..134980767hg38UCSC Ensembl
Innerchr11:134710969..134850661hg19UCSC Ensembl
Innerchr11:134216179..134355871hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38139693
hg19139693
hg18139693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1315n100
Supporting Variantsnssv3710792, nssv3518515
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)nsv1048893
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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