A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1027n100



Internal ID22787114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4926918..4952787hg38UCSC Ensembl
chr11:4948148..4974017hg19UCSC Ensembl
chr11:4904724..4930593hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825870
hg1925870
hg1825870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044434, nsv1036758, nsv1049277, nsv1047179, nsv1052130
Samples
Known GenesOR51A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1027n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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