A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661814



Internal ID9581233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8848421..8848595hg38UCSC Ensembl
Outerchr17:8848384..8848645hg38UCSC Ensembl
Innerchr17:8751738..8751912hg19UCSC Ensembl
Outerchr17:8751701..8751962hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6055098
SamplesNA19225
Known GenesPIK3R6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661814
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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