A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1110n100



Internal ID22787197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45433881..45465681hg38UCSC Ensembl
chr11:45455431..45487231hg19UCSC Ensembl
chr11:45412007..45443807hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3831801
hg1931801
hg1831801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050657, nsv1035430, nsv1035254
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)dgv1110n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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