A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893212



Internal ID19184032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43057570..43089269hg38UCSC Ensembl
Outerchr19:43052691..43089269hg38UCSC Ensembl
Innerchr19:43561722..43593421hg19UCSC Ensembl
Outerchr19:43556843..43593421hg19UCSC Ensembl
Innerchr19:48253562..48285261hg18UCSC Ensembl
Outerchr19:48248683..48285261hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3836579
hg1936579
hg1836579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778357, essv25786996, essv25798808
Samples
Known GenesPSG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893212
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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