A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996789



Internal ID6732731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45568395..45568809hg38UCSC Ensembl
chr3:45609887..45610301hg19UCSC Ensembl
chr3:45584891..45585305hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38415
hg19415
hg18415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv106e180
Supporting Variantsessv3578925
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996789
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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