A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3585n100



Internal ID22789672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43029263..43285762hg38UCSC Ensembl
chr19:43533415..43789914hg19UCSC Ensembl
chr19:48225255..48481754hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38256500
hg19256500
hg18256500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065551, nsv1062359, nsv1064219, nsv1067157, nsv1066647, nsv1061734, nsv1059244, nsv1056735, nsv1055822, nsv1056428, nsv1062295, nsv1065978
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3585n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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