A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990309



Internal ID6726277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98502683..98517911hg38UCSC Ensembl
Outerchr15:99045912..99061140hg19UCSC Ensembl
Outerchr15:96863435..96878663hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3815229
hg1915229
hg1815229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564355
SamplesHuRef
Known GenesFAM169B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990309
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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