A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1268n54



Internal ID20134692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76494954..76505371hg38UCSC Ensembl
chr10:78254712..78265129hg19UCSC Ensembl
chr10:77924718..77935135hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3810418
hg1910418
hg1810418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551541, nsv551545
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1268n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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