A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566995



Internal ID18768071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170040691..170040928hg38UCSC Ensembl
Outerchr5:170040657..170040980hg38UCSC Ensembl
Innerchr5:169467695..169467932hg19UCSC Ensembl
Outerchr5:169467661..169467984hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765742
Samples
Known GenesDOCK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566995
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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