A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1259n100



Internal ID22787346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97428102..97509648hg38UCSC Ensembl
chr11:97299102..97380648hg19UCSC Ensembl
chr11:96804312..96885858hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3881547
hg1981547
hg1881547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054880, nsv1055058
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)dgv1259n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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