A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275238



Internal ID348144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98414748..98416514hg38UCSC Ensembl
Outerchr14:98408253..98417197hg38UCSC Ensembl
Innerchr14:98881085..98882851hg19UCSC Ensembl
Outerchr14:98874590..98883534hg19UCSC Ensembl
Innerchr14:97950838..97952604hg18UCSC Ensembl
Outerchr14:97944343..97953287hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388945
hg198945
hg188945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585955
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)esv275238
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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