A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564101



Internal ID18418491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76027519..76027718hg38UCSC Ensembl
Outerchr4:76027457..76027764hg38UCSC Ensembl
Innerchr4:76948672..76948871hg19UCSC Ensembl
Outerchr4:76948610..76948917hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762848
Samples
Known GenesART3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564101
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