A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565456



Internal ID7036838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86406101..86409538hg38UCSC Ensembl
Outerchr9:89021016..89024453hg19UCSC Ensembl
Outerchr9:88210836..88214273hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384112
hg194112
hg184112
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005962
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565456
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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