A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586954



Internal ID7058336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41227775..41237595hg38UCSC Ensembl
Innerchr17:39384027..39393847hg19UCSC Ensembl
Innerchr17:36637553..36647373hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg389821
hg199821
hg189821
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991633
Supporting Variants
SamplesHuRef
Known GenesKRTAP9-3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586954
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer