A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564457



Internal ID18418847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113213969..113214397hg38UCSC Ensembl
Outerchr4:113213863..113214470hg38UCSC Ensembl
Innerchr4:114135125..114135553hg19UCSC Ensembl
Outerchr4:114135019..114135626hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763204
Samples
Known GenesANK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564457
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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