A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753486



Internal ID18727732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71856014..71856309hg38UCSC Ensembl
Outerchr17:71855968..71856373hg38UCSC Ensembl
Innerchr17:69852155..69852450hg19UCSC Ensembl
Outerchr17:69852109..69852514hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753486
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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