A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994498



Internal ID6730451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86998975..86999261hg38UCSC Ensembl
Outerchr9:89613890..89614176hg19UCSC Ensembl
Outerchr9:88803710..88803996hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382800
hg192800
hg182800
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565444
SamplesHuRef
Known GenesLOC100506834
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994498
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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