A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585656



Internal ID347235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53390229..53390840hg38UCSC Ensembl
Outerchr15:53390171..53391106hg38UCSC Ensembl
Innerchr15:53682426..53683037hg19UCSC Ensembl
Outerchr15:53682368..53683303hg19UCSC Ensembl
Innerchr15:51469718..51470329hg18UCSC Ensembl
Outerchr15:51469660..51470595hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38936
hg19936
hg18936
Variant TypeOTHER complex
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275223
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)essv2585656
Frequency
Sample Size1250
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer