A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5469n100



Internal ID22791556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170321038..170368212hg38UCSC Ensembl
chr4:171242189..171289363hg19UCSC Ensembl
chr4:171478764..171525938hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3847175
hg1947175
hg1847175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019263, nsv1028444, nsv1015999, nsv1026920
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)dgv5469n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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