A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1248n100



Internal ID22787335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86172261..86187767hg38UCSC Ensembl
chr11:85883303..85898809hg19UCSC Ensembl
chr11:85560951..85576457hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3815507
hg1915507
hg1815507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049881, nsv1049658, nsv1043422, nsv1040400
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)dgv1248n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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