A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1128n100



Internal ID20152744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49670632..50810134hg38UCSC Ensembl
chr11:49692184..50769305hg19UCSC Ensembl
chr11:49648760..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381139503
hg191077122
hg181077122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051021, nsv1036701
Samples
Known GenesLOC440040, LOC441601, LOC646813, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1128n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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