A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994946



Internal ID7079481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134848784..134850929hg38UCSC Ensembl
Innerchr9:137740630..137742775hg19UCSC Ensembl
Innerchr9:136880451..136882596hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382146
hg192146
hg182146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586431
SamplesHuRef
Known GenesLOC101448202, MIR3689A, MIR3689B, MIR3689C, MIR3689D1, MIR3689D2, MIR3689E, MIR3689F
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994946
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