A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662692



Internal ID9582111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74883472..74884348hg38UCSC Ensembl
Outerchr17:74883315..74884501hg38UCSC Ensembl
Innerchr17:72879602..72880478hg19UCSC Ensembl
Outerchr17:72879445..72880631hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6207130
SamplesNA18501
Known GenesFADS6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662692
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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