A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753601



Internal ID18727847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80355343..80355656hg38UCSC Ensembl
Outerchr17:80355301..80355729hg38UCSC Ensembl
Innerchr17:78329143..78329456hg19UCSC Ensembl
Outerchr17:78329101..78329529hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554854
Supporting Variants
Samples
Known GenesLOC100294362, RNF213
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753601
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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