A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3485n100



Internal ID22789572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:24196288..24338821hg38UCSC Ensembl
chr19:24379090..24521623hg19UCSC Ensembl
chr19:24170930..24313463hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38142534
hg19142534
hg18142534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064250, nsv1057596, nsv1066978, nsv1062273
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)dgv3485n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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