A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566103



Internal ID18767179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74887064..74891055hg38UCSC Ensembl
Outerchr5:74886176..74892175hg38UCSC Ensembl
Innerchr5:74182889..74186880hg19UCSC Ensembl
Outerchr5:74182001..74188000hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764850
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566103
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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