A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554779



Internal ID18409169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74877367..74881676hg38UCSC Ensembl
Outerchr17:74876872..74881870hg38UCSC Ensembl
Innerchr17:72873496..72877806hg19UCSC Ensembl
Outerchr17:72873001..72878000hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384999
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753526
Samples
Known GenesFADS6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554779
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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