A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565802



Internal ID18420192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35191055..35191330hg38UCSC Ensembl
Outerchr5:35191002..35191403hg38UCSC Ensembl
Innerchr5:35191157..35191432hg19UCSC Ensembl
Outerchr5:35191104..35191505hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764549
Samples
Known GenesPRLR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565802
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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