A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893210



Internal ID19184030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42897784..43009507hg38UCSC Ensembl
Outerchr19:42867142..43076596hg38UCSC Ensembl
Innerchr19:43401936..43513659hg19UCSC Ensembl
Outerchr19:43371294..43580748hg19UCSC Ensembl
Innerchr19:48093776..48205499hg18UCSC Ensembl
Outerchr19:48063134..48272588hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38209455
hg19209455
hg18209455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796396, essv25797131, essv25796121, essv25797477, essv25797566, essv25797396, essv25797634, essv25798068, essv25797641, essv25797588, essv25797949, essv25796771, essv25796999, essv25798035, essv25796938, essv25797101, essv25796491, essv25796597, essv25796352, essv25796241, essv25798009, essv25796546, essv25798019, essv25796946, essv25796211, essv25798079, essv25798013, essv25797168, essv25796712, essv25796243, essv25797764, essv25796783, essv25787728
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893210
Frequency
Sample Size3017
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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