A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585166



Internal ID346745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19638834..19641884hg38UCSC Ensembl
Outerchr7:19637912..19642525hg38UCSC Ensembl
Innerchr7:19678457..19681507hg19UCSC Ensembl
Outerchr7:19677535..19682148hg19UCSC Ensembl
Innerchr7:19644982..19648032hg18UCSC Ensembl
Outerchr7:19644060..19648673hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384614
hg194614
hg184614
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274895
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)essv2585166
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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