A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998326



Internal ID6734262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068881..152071025hg38UCSC Ensembl
Innerchr6:152390016..152392160hg19UCSC Ensembl
Innerchr6:152431709..152433853hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382145
hg192145
hg182145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv164e180
Supporting Variantsessv3586961
SamplesHuRef
Known GenesESR1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998326
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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