A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764338



Internal ID18391898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17343088..17356858hg38UCSC Ensembl
Outerchr5:17340892..17357788hg38UCSC Ensembl
Innerchr5:17343197..17356967hg19UCSC Ensembl
Outerchr5:17341001..17357897hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3816897
hg1916897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764338
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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