A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275313



Internal ID1533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69199164..69200152hg38UCSC Ensembl
Outerchr9:69198655..69200237hg38UCSC Ensembl
Innerchr9:71814080..71815068hg19UCSC Ensembl
Outerchr9:71813571..71815153hg19UCSC Ensembl
Innerchr9:71003900..71004888hg18UCSC Ensembl
Outerchr9:71003391..71004973hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381583
hg191583
hg181583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585652
Samples
Known GenesTJP2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275313
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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