A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990890



Internal ID7077021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:10977190..10983982hg38UCSC Ensembl
Outerchr2:11117316..11124108hg19UCSC Ensembl
Outerchr2:11034767..11041559hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386793
hg196793
hg186793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565463
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990890
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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