A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659855



Internal ID9579274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74162544..74240352hg38UCSC Ensembl
Outerchr10:74162507..74240402hg38UCSC Ensembl
Innerchr10:75922302..76000110hg19UCSC Ensembl
Outerchr10:75922265..76000160hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3877896
hg1977896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5414498
SamplesHG01069
Known GenesADK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659855
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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