A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586513



Internal ID6711209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109673918..109701984hg38UCSC Ensembl
Innerchr1:110216540..110244606hg19UCSC Ensembl
Innerchr1:110018063..110046129hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3828067
hg1928067
hg1828067
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998761
Supporting Variants
SamplesHuRef
Known GenesGSTM1, GSTM2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586513
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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