A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1106n54



Internal ID20134530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46385067..46489856hg38UCSC Ensembl
chr10:47028331..47164700hg19UCSC Ensembl
chr10:46448337..46584706hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38104790
hg19136370
hg18136370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550724, nsv550727
Samples
Known GenesANXA8, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1106n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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