A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563972



Internal ID6688355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101677673..101686359hg38UCSC Ensembl
Outerchr15:102217876..102226562hg19UCSC Ensembl
Outerchr15:100035399..100044085hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388687
hg198687
hg188687
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005771
Supporting Variants
SamplesHuRef
Known GenesTARSL2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563972
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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