A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989763



Internal ID7076348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133296205..133322140hg38UCSC Ensembl
Outerchr9:136171778..136188976hg19UCSC Ensembl
Outerchr9:135161599..135178797hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3810896
hg1910896
hg1810896
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565372
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989763
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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