A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1297n100



Internal ID20152913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131036593..131374908hg38UCSC Ensembl
chr11:130906488..131244803hg19UCSC Ensembl
chr11:130411698..130750013hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38338316
hg19338316
hg18338316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038442, nsv1044260, nsv1041781, nsv1050347
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1297n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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