A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659410



Internal ID9925516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31845625..31854231hg38UCSC Ensembl
Outerchr10:31845588..31854281hg38UCSC Ensembl
Innerchr10:32134553..32143159hg19UCSC Ensembl
Outerchr10:32134516..32143209hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388694
hg198694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5448371
SamplesHG00589
Known GenesARHGAP12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659410
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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