A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556125



Internal ID18757201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17745410..17745967hg38UCSC Ensembl
Outerchr19:17745297..17745994hg38UCSC Ensembl
Innerchr19:17856219..17856776hg19UCSC Ensembl
Outerchr19:17856106..17856803hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754872
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556125
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