A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1076n100



Internal ID22787163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25067166..25115199hg38UCSC Ensembl
chr11:25088712..25136745hg19UCSC Ensembl
chr11:25045288..25093321hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3848034
hg1948034
hg1848034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046075, nsv1041328
Samples
Known GenesLUZP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1076n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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