A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669291



Internal ID9588710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26468348..26476526hg38UCSC Ensembl
Outerchr10:26468311..26476576hg38UCSC Ensembl
Innerchr10:26757277..26765455hg19UCSC Ensembl
Outerchr10:26757240..26765505hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388266
hg198266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5535722
SamplesHG00543
Known GenesAPBB1IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669291
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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