A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005771



Internal ID6717891
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563972
SamplesHuRef
Known GenesTARSL2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005771
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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