A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998828



Internal ID7064581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:11428306..11436848hg38UCSC Ensembl
Outerchr3:11469780..11478322hg19UCSC Ensembl
Outerchr3:11444780..11453322hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388543
hg198543
hg188543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564697
SamplesHuRef
Known GenesATG7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998828
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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