A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1234n100



Internal ID20152850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77572991..77724786hg38UCSC Ensembl
chr11:77284036..77435831hg19UCSC Ensembl
chr11:76961684..77113479hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38151796
hg19151796
hg18151796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048892, nsv1035494, nsv1053074, nsv1038974
Samples
Known GenesAQP11, CLNS1A, RSF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1234n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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