A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586465



Internal ID6711161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59582954..59583986hg38UCSC Ensembl
Innerchr1:60048626..60049658hg19UCSC Ensembl
Innerchr1:59821214..59822246hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381033
hg191033
hg181033
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994342
Supporting Variants
SamplesHuRef
Known GenesFGGY
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586465
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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