A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586606



Internal ID7057988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550773..31552343hg38UCSC Ensembl
Innerchr7:31590387..31591957hg19UCSC Ensembl
Innerchr7:31556912..31558482hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381571
hg191571
hg181571
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005712
Supporting Variants
SamplesHuRef
Known GenesCCDC129
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586606
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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