A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005787



Internal ID6717907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42989602..42989929hg38UCSC Ensembl
chr3:43031094..43031421hg19UCSC Ensembl
chr3:43006098..43006425hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38328
hg19328
hg18328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3583427
SamplesHuRef
Known GenesFAM198A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005787
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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