A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3581n100



Internal ID22789668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42971344..43139226hg38UCSC Ensembl
chr19:43475496..43643378hg19UCSC Ensembl
chr19:48167336..48335218hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38167883
hg19167883
hg18167883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064346, nsv1060996, nsv1060797, nsv1063507, nsv1059321, nsv1063373, nsv1055451, nsv1057908
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3581n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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