A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3508n100



Internal ID22789595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28001812..28215779hg38UCSC Ensembl
chr19:28492719..28706686hg19UCSC Ensembl
chr19:33184559..33398526hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38213968
hg19213968
hg18213968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056954, nsv1062160
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)dgv3508n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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