A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3468n100



Internal ID20155084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20643872..20759686hg38UCSC Ensembl
chr19:20826678..20942492hg19UCSC Ensembl
chr19:20618518..20734332hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38115815
hg19115815
hg18115815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058833, nsv1060213, nsv1057408
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3468n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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