A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565420



Internal ID18766496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3502216..3502522hg38UCSC Ensembl
Outerchr5:3502149..3502578hg38UCSC Ensembl
Innerchr5:3502330..3502636hg19UCSC Ensembl
Outerchr5:3502263..3502692hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764167
Samples
Known GenesLINC01019, LOC102467075
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565420
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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