A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565371



Internal ID18766447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1682400..1682655hg38UCSC Ensembl
Outerchr5:1682328..1682691hg38UCSC Ensembl
Innerchr5:1682515..1682770hg19UCSC Ensembl
Outerchr5:1682443..1682806hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764118
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565371
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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