A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3127567



Internal ID11147233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89483670..89483734hg38UCSC Ensembl
chr9:92098585..92098649hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7397134
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3127567
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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