A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564527



Internal ID18765603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119944374..119945260hg38UCSC Ensembl
Outerchr4:119944342..119945470hg38UCSC Ensembl
Innerchr4:120865529..120866415hg19UCSC Ensembl
Outerchr4:120865497..120866625hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763274
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564527
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