A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007815



Internal ID7072909
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586872
SamplesHuRef
Known GenesHLA-DRB5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007815
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