A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv38n50



Internal ID22767867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141853145..141854921hg38UCSC Ensembl
chr3:141571987..141573763hg19UCSC Ensembl
chr3:143054677..143056453hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381777
hg191777
hg181777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv511222, nsv513080
Samples1
Known Genes
MethodSequencing
SNP array
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Not reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv38n50
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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