A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1260n100



Internal ID22787347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98056829..98412123hg38UCSC Ensembl
chr11:97927557..98282852hg19UCSC Ensembl
chr11:97432767..97788062hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38355295
hg19355296
hg18355296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035193, nsv1049076
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)dgv1260n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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