A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3566n100



Internal ID22789653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42786621..43307659hg38UCSC Ensembl
chr19:43290773..43811811hg19UCSC Ensembl
chr19:47982613..48503651hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38521039
hg19521039
hg18521039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066912, nsv1066021, nsv1065736, nsv1059067, nsv1060784, nsv1064999
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3566n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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