A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1098n100



Internal ID22787185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37380066..37427833hg38UCSC Ensembl
chr11:37401616..37449383hg19UCSC Ensembl
chr11:37358192..37405959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3847768
hg1947768
hg1847768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053725, nsv1051916
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)dgv1098n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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