A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275074



Internal ID347980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129098428..129098847hg38UCSC Ensembl
Outerchr7:129097524..129101980hg38UCSC Ensembl
Innerchr7:128738482..128738901hg19UCSC Ensembl
Outerchr7:128737578..128742034hg19UCSC Ensembl
Innerchr7:128525718..128526137hg18UCSC Ensembl
Outerchr7:128524814..128529270hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg384457
hg194457
hg184457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585428
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)esv275074
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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