A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667444



Internal ID9933549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89062379..89071310hg38UCSC Ensembl
Outerchr10:89062345..89071345hg38UCSC Ensembl
Innerchr10:90822136..90831067hg19UCSC Ensembl
Outerchr10:90822102..90831102hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv160e199
Supporting Variantsessv6300445
SamplesHG00554
Known GenesMIR4679-1, MIR4679-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667444
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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