A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997828



Internal ID7064049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89211912..89212504hg38UCSC Ensembl
Innerchr6:89921631..89922223hg19UCSC Ensembl
Innerchr6:89978350..89978942hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586208
SamplesHuRef
Known GenesGABRR1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997828
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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