A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3583n100



Internal ID22789670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42999122..43264030hg38UCSC Ensembl
chr19:43503274..43768182hg19UCSC Ensembl
chr19:48195114..48460022hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38264909
hg19264909
hg18264909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057345, nsv1066084, nsv1063261, nsv1062655, nsv1066555, nsv1059634, nsv1055564, nsv1067032, nsv1066574, nsv1063449, nsv1057651, nsv1058384, nsv1061294, nsv1055881, nsv1055832, nsv1065672, nsv1059245, nsv1064147, nsv1056128, nsv1059235, nsv1060095, nsv1061441, nsv1061839, nsv1066296, nsv1061386, nsv1066720, nsv1063562, nsv1055968
Samples
Known GenesLOC284344, PSG11, 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)dgv3583n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer