A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv164e180



Internal ID20123103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152068853..152071075hg38UCSC Ensembl
chr6:152389988..152392210hg19UCSC Ensembl
chr6:152431681..152433903hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382223
hg192223
hg182223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv998326, esv1004724
SamplesHuRef
Known GenesESR1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv164e180
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