A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587277



Internal ID7058659
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004094
Supporting Variants
SamplesHuRef
Known GenesGSTM1, GSTM2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587277
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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