A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5359n100



Internal ID22791446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113433086..113444560hg38UCSC Ensembl
chr4:114354242..114365716hg19UCSC Ensembl
chr4:114573691..114585165hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3811475
hg1911475
hg1811475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011483, nsv1000299
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5359n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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