A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004724



Internal ID6716847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068853..152071075hg38UCSC Ensembl
Innerchr6:152389988..152392210hg19UCSC Ensembl
Innerchr6:152431681..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 Variantsdgv164e180
Supporting Variantsessv3586584
SamplesHuRef
Known GenesESR1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004724
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