A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586686



Internal ID7058068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61071794..61073576hg38UCSC Ensembl
Innerchr7:61054519..61056301hg19UCSC Ensembl
Innerchr7:61058461..61060243hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381783
hg191783
hg181783
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997723
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586686
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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