A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3584966



Internal ID7056348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100511533..100511971hg38UCSC Ensembl
chr15:101051738..101052176hg19UCSC Ensembl
chr15:98869261..98869699hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38439
hg19439
hg18439
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990393
Supporting Variants
SamplesHuRef
Known GenesCERS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3584966
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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