A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668020



Internal ID9934125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130429686..130429796hg38UCSC Ensembl
Innerchr9:133305073..133305183hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5507870
SamplesNA12878
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668020
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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