A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275165



Internal ID1385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41496256..41496274hg38UCSC Ensembl
Outerchr21:41496192..41496398hg38UCSC Ensembl
Innerchr21:42868183..42868201hg19UCSC Ensembl
Outerchr21:42868119..42868325hg19UCSC Ensembl
Innerchr21:41790053..41790071hg18UCSC Ensembl
Outerchr21:41789989..41790195hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38207
hg19207
hg18207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585173
Samples
Known GenesTMPRSS2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275165
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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