A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990800



Internal ID7076931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:156025243..156036581hg38UCSC Ensembl
Outerchr2:156881755..156893093hg19UCSC Ensembl
Outerchr2:156590001..156601339hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3811339
hg1911339
hg1811339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564739
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990800
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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