A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765186



Internal ID18739432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109487922..109490418hg38UCSC Ensembl
Outerchr5:109487773..109490474hg38UCSC Ensembl
Innerchr5:108823623..108826119hg19UCSC Ensembl
Outerchr5:108823474..108826175hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765186
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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