A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565419



Internal ID18766495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3499214..3499447hg38UCSC Ensembl
Outerchr5:3499149..3499486hg38UCSC Ensembl
Innerchr5:3499328..3499561hg19UCSC Ensembl
Outerchr5:3499263..3499600hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv347e215
Supporting Variantsessv9764166
Samples
Known GenesLINC01019, LOC102467075
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565419
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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