A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586584



Internal ID6711280
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004724
Supporting Variants
SamplesHuRef
Known GenesESR1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586584
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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