A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1242n100



Internal ID22787329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81725388..81884472hg38UCSC Ensembl
chr11:81436430..81595514hg19UCSC Ensembl
chr11:81114078..81273162hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38159085
hg19159085
hg18159085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039927, nsv1035910
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)dgv1242n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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