A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3435n100



Internal ID22789522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12405336..12451697hg38UCSC Ensembl
chr19:12516150..12562511hg19UCSC Ensembl
chr19:12377150..12423511hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3846362
hg1946362
hg1846362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066999, nsv1063309, nsv1057865, nsv1056292
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3435n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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