A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3684n100



Internal ID22789771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57477028..57492505hg38UCSC Ensembl
chr19:57988396..58003873hg19UCSC Ensembl
chr19:62680208..62695685hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815478
hg1915478
hg1815478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055327, nsv1058182, nsv1062918
Samples
Known GenesZNF419, ZNF772
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3684n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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