A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585281



Internal ID346860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26806677..26808189hg38UCSC Ensembl
Outerchr13:26803084..26808880hg38UCSC Ensembl
Innerchr13:27380814..27382326hg19UCSC Ensembl
Outerchr13:27377221..27383017hg19UCSC Ensembl
Innerchr13:26278814..26280326hg18UCSC Ensembl
Outerchr13:26275221..26281017hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg385797
hg195797
hg185797
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274996
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)essv2585281
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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