A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554561



Internal ID18755637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54082140..54090139hg38UCSC Ensembl
Outerchr17:54080140..54090729hg38UCSC Ensembl
Innerchr17:52159501..52167500hg19UCSC Ensembl
Outerchr17:52157501..52168090hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810590
hg1910590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753308
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554561
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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