A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586209



Internal ID7057591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41227954..41238044hg38UCSC Ensembl
Innerchr17:39384206..39394296hg19UCSC Ensembl
Innerchr17:36637732..36647822hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3810091
hg1910091
hg1810091
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990862
Supporting Variants
SamplesHuRef
Known GenesKRTAP9-3, KRTAP9-8
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586209
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