A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621931



Internal ID6662107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133063192..133080639hg38UCSC Ensembl
chr9:135938579..135956026hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3817448
hg1917448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13638926, essv13638924, essv13638927, essv13638916, essv13638917, essv13638921, essv13638920, essv13638925, essv13638923, essv13638922, essv13638919, essv13638918, essv13638928
SamplesHG02150, HG04002, HG04018, NA18627, HG02595, HG00260, HG03428, HG03969, HG00476, HG01108, HG01804, HG03410, HG02406
Known GenesCEL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621931
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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