A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9606n54



Internal ID22777501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14581657..14582222hg38UCSC Ensembl
chr5:14581766..14582331hg19UCSC Ensembl
chr5:14634766..14635331hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38566
hg19566
hg18566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597243, nsv597248
Samples
Known GenesFAM105A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9606n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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