A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752708



Internal ID18726954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:898409..898978hg38UCSC Ensembl
Outerchr17:898338..899120hg38UCSC Ensembl
Innerchr17:801649..802218hg19UCSC Ensembl
Outerchr17:801578..802360hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553961
Supporting Variants
Samples
Known GenesNXN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752708
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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