A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040135



Internal ID19129354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96736288..96927717hg38UCSC Ensembl
Innerchr11:96607288..96798717hg19UCSC Ensembl
Innerchr11:96112498..96303927hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38191430
hg19191430
hg18191430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511787
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)nsv1040135
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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