A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667357



Internal ID9586776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43887894..43888638hg38UCSC Ensembl
chr10:44383342..44384086hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5977906, essv6139933, essv5562264, essv6007052, essv5875872, essv5703862, essv6249803, essv6457975, essv5462077
SamplesNA18870, HG01359, NA19383, NA19239, NA18856, NA19398, NA06986, NA19240, NA18980
Known GenesLINC00840
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667357
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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