A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv30n50



Internal ID22767859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8678934..8728561hg38UCSC Ensembl
chr3:8720620..8770247hg19UCSC Ensembl
chr3:8695620..8745247hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3849628
hg1949628
hg1849628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv511207, nsv513034
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)dgv30n50
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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