A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994482



Internal ID7079132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:60070..82205hg38UCSC Ensembl
Innerchr19:60070..82205hg19UCSC Ensembl
Innerchr19:11070..33205hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3822136
hg1922136
hg1822136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586674
SamplesHuRef
Known GenesFAM138A, FAM138F, WASH5P
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994482
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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