A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565761



Internal ID18766837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31677333..31677636hg38UCSC Ensembl
Outerchr5:31677274..31677694hg38UCSC Ensembl
Innerchr5:31677440..31677743hg19UCSC Ensembl
Outerchr5:31677381..31677801hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764508
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565761
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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