A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585532



Internal ID347111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97317178..97317387hg38UCSC Ensembl
Outerchr7:97317057..97339016hg38UCSC Ensembl
Innerchr7:96946490..96946699hg19UCSC Ensembl
Outerchr7:96946369..96968328hg19UCSC Ensembl
Innerchr7:96784426..96784635hg18UCSC Ensembl
Outerchr7:96784305..96806264hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3821960
hg1921960
hg1821960
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274910
Supporting Variants
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)essv2585532
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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