A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052457



Internal ID19141676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106606872..106636471hg38UCSC Ensembl
Innerchr11:106477599..106507197hg19UCSC Ensembl
Innerchr11:105982809..106012407hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3829600
hg1929599
hg1829599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520017
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)nsv1052457
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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