A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566696



Internal ID18767772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:137845903..137852260hg38UCSC Ensembl
Outerchr5:137845312..137852773hg38UCSC Ensembl
Innerchr5:137181592..137187949hg19UCSC Ensembl
Outerchr5:137181001..137188462hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg387462
hg197462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765443
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566696
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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