A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753106



Internal ID18727352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35561855..35562088hg38UCSC Ensembl
Outerchr17:35561800..35562131hg38UCSC Ensembl
Innerchr17:33888874..33889107hg19UCSC Ensembl
Outerchr17:33888819..33889150hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753106
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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