A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562984



Internal ID18764060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180514207..180514248hg38UCSC Ensembl
Outerchr3:180514203..180514252hg38UCSC Ensembl
Innerchr3:180231995..180232036hg19UCSC Ensembl
Outerchr3:180231991..180232040hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761731
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562984
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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