A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3739487



Internal ID11675697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131952097..131952216hg38UCSC Ensembl
chr10:133765601..133765720hg19UCSC Ensembl
chr10:133615591..133615710hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38120
hg19120
hg18120
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1363864
Supporting Variants
SamplesHuRef
Known GenesPPP2R2D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3739487
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer