A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003434



Internal ID7068540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681762..109700331hg38UCSC Ensembl
Innerchr1:110224384..110242953hg19UCSC Ensembl
Innerchr1:110025907..110044476hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818570
hg1918570
hg1818570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6e180
Supporting Variantsessv3586031
SamplesHuRef
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003434
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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