A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564780



Internal ID6689476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:65139616..65150605hg38UCSC Ensembl
Outerchr17:63135734..63146723hg19UCSC Ensembl
Outerchr17:60566196..60577185hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3810990
hg1910990
hg1810990
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009898
Supporting Variants
SamplesHuRef
Known GenesRGS9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564780
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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