A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3931706



Internal ID11830166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34528026..34528359hg38UCSC Ensembl
chr20:33115831..33116164hg19UCSC Ensembl
chr20:32579492..32579825hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38334
hg19334
hg18334
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1132908
Supporting Variants
SamplesHuRef
Known GenesDYNLRB1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3931706
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