A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3267829



Internal ID10940809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123206..69128440hg38UCSC Ensembl
Outerchr9:71738122..71743356hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38e209
Supporting Variantsessv7537396
SamplesHuRef
Known GenesTJP2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3267829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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