A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586872



Internal ID7058254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32524942..32529353hg38UCSC Ensembl
Innerchr6:32492719..32497130hg19UCSC Ensembl
Innerchr6:32600697..32605108hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384412
hg194412
hg184412
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007815
Supporting Variants
SamplesHuRef
Known GenesHLA-DRB5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586872
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