A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564196



Internal ID18418586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87111006..87111293hg38UCSC Ensembl
Outerchr4:87110937..87111370hg38UCSC Ensembl
Innerchr4:88032158..88032445hg19UCSC Ensembl
Outerchr4:88032089..88032522hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762943
Samples
Known GenesAFF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564196
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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