A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585494



Internal ID347073
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274920
Supporting Variants
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)essv2585494
Frequency
Sample Size1250
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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