A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566698



Internal ID18767774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138108302..138108517hg38UCSC Ensembl
Outerchr5:138108291..138108555hg38UCSC Ensembl
Innerchr5:137443991..137444206hg19UCSC Ensembl
Outerchr5:137443980..137444244hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765445
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566698
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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