A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565854



Internal ID18766930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41603899..41604205hg38UCSC Ensembl
Outerchr5:41603849..41604285hg38UCSC Ensembl
Innerchr5:41604001..41604307hg19UCSC Ensembl
Outerchr5:41603951..41604387hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv355e215
Supporting Variantsessv9764601
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565854
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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