A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660277



Internal ID9926382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73763458..73771834hg38UCSC Ensembl
Outerchr17:73763421..73771884hg38UCSC Ensembl
Innerchr17:71759597..71767973hg19UCSC Ensembl
Outerchr17:71759560..71768023hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388464
hg198464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5445920
SamplesNA19652
Known GenesLINC00469
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660277
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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