A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563476



Internal ID18764552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16942714..16949117hg38UCSC Ensembl
Outerchr4:16942608..16949144hg38UCSC Ensembl
Innerchr4:16944337..16950740hg19UCSC Ensembl
Outerchr4:16944231..16950767hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386537
hg196537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762223
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563476
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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