A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037438



Internal ID19126657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128784349..128806065hg38UCSC Ensembl
Innerchr11:128654244..128675960hg19UCSC Ensembl
Innerchr11:128159454..128181170hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3821717
hg1921717
hg1821717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505009
Samples
Known GenesFLI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037438
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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