A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666683



Internal ID9932788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208477..112210460hg38UCSC Ensembl
chr9:114970757..114972740hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381984
hg191984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6129103, essv5837815, essv6289701, essv6509202, essv5711290, essv5588336, essv5713408, essv5805083, essv5774631, essv5525924, essv5531258, essv6523833, essv5780425, essv6109766, essv6518231, essv6055744
SamplesNA18510, NA18519, NA19201, NA18498, NA19209, NA18910, NA18499, NA18853, NA19395, NA19440, NA19144, NA19835, NA19428, NA19472, NA19093, NA19129
Known GenesMIR3134
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666683
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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