A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751856



Internal ID12638722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:242317308..242730382hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17413075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv165e55
Supporting Variantsessv6989810, essv6989373
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751856
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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