A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563874



Internal ID6688257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123108..69128559hg38UCSC Ensembl
Outerchr9:71738024..71743475hg19UCSC Ensembl
Outerchr9:70927844..70933295hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385452
hg195452
hg185452
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005385
Supporting Variants
SamplesHuRef
Known GenesTJP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563874
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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