A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566304



Internal ID18767380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96630842..96631478hg38UCSC Ensembl
Outerchr5:96630734..96631672hg38UCSC Ensembl
Innerchr5:95966546..95967182hg19UCSC Ensembl
Outerchr5:95966438..95967376hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765051
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566304
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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