A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274905



Internal ID347865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78081973..78084596hg38UCSC Ensembl
Outerchr7:78081766..78087304hg38UCSC Ensembl
Innerchr7:77711290..77713913hg19UCSC Ensembl
Outerchr7:77711083..77716621hg19UCSC Ensembl
Innerchr7:77549226..77551849hg18UCSC Ensembl
Outerchr7:77549019..77554557hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg385539
hg195539
hg185539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585186
Samples
Known GenesMAGI2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274905
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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