A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755220



Internal ID18729466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46120113..46124539hg38UCSC Ensembl
Outerchr19:46119244..46125243hg38UCSC Ensembl
Innerchr19:46623370..46627796hg19UCSC Ensembl
Outerchr19:46622501..46628500hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556473
Supporting Variants
Samples
Known GenesIGFL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755220
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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