A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275177



Internal ID348083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103342596..103343065hg38UCSC Ensembl
Outerchr9:103340870..103349909hg38UCSC Ensembl
Innerchr9:106104878..106105347hg19UCSC Ensembl
Outerchr9:106103152..106112191hg19UCSC Ensembl
Innerchr9:105144699..105145168hg18UCSC Ensembl
Outerchr9:105142973..105152012hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389040
hg199040
hg189040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586007
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275177
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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