A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565609



Internal ID7036991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:206837505..206845282hg38UCSC Ensembl
Outerchr1:207010850..207018627hg19UCSC Ensembl
Outerchr1:205077473..205085250hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387778
hg197778
hg187778
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997006
Supporting Variants
SamplesHuRef
Known GenesIL19
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565609
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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