A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274920



Internal ID347880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45687729..45688194hg38UCSC Ensembl
Outerchr15:45685162..45688336hg38UCSC Ensembl
Innerchr15:45979927..45980392hg19UCSC Ensembl
Outerchr15:45977360..45980534hg19UCSC Ensembl
Innerchr15:43767219..43767684hg18UCSC Ensembl
Outerchr15:43764652..43767826hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383175
hg193175
hg183175
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585494
Samples
Known GenesSQRDL
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274920
Frequency
Sample Size1250
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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