A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004094



Internal ID7069196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109678923..109697767hg38UCSC Ensembl
Innerchr1:110221545..110240389hg19UCSC Ensembl
Innerchr1:110023068..110041912hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818845
hg1918845
hg1818845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6e180
Supporting Variantsessv3587277
SamplesHuRef
Known GenesGSTM1, GSTM2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004094
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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