A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009447



Internal ID7059376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30601457..30601791hg38UCSC Ensembl
chr13:31175594..31175928hg19UCSC Ensembl
chr13:30073594..30073928hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38335
hg19335
hg18335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3571943
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009447
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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