A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666028



Internal ID9932133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17362859..17370503hg38UCSC Ensembl
Outerchr17:17362822..17370553hg38UCSC Ensembl
Innerchr17:17266173..17273817hg19UCSC Ensembl
Outerchr17:17266136..17273867hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg387732
hg197732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6399772
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666028
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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