A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586361



Internal ID6711057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179638222..179638890hg38UCSC Ensembl
Innerchr1:179607357..179608025hg19UCSC Ensembl
Innerchr1:177873980..177874648hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38669
hg19669
hg18669
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997488
Supporting Variants
SamplesHuRef
Known GenesTDRD5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586361
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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