A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554814



Internal ID18409204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77267919..77277089hg38UCSC Ensembl
Outerchr17:77267106..77277918hg38UCSC Ensembl
Innerchr17:75264001..75273171hg19UCSC Ensembl
Outerchr17:75263188..75274000hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3810813
hg1910813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753561
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554814
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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