A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564468



Internal ID18765544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114847085..114847410hg38UCSC Ensembl
Outerchr4:114847059..114847452hg38UCSC Ensembl
Innerchr4:115768241..115768566hg19UCSC Ensembl
Outerchr4:115768215..115768608hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763215
Samples
Known GenesNDST4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564468
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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