A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5190n100



Internal ID22791277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35369560..35409909hg38UCSC Ensembl
chr4:35371182..35411531hg19UCSC Ensembl
chr4:35047577..35087926hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3840350
hg1940350
hg1840350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005307, nsv1014543, nsv1005722
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)dgv5190n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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