A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1746393



Internal ID12909511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5962354..5962683hg38UCSC Ensembl
chr20:5943000..5943329hg19UCSC Ensembl
chr20:5891000..5891329hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38330
hg19330
hg18330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4296076
SamplesHuRef
Known GenesMCM8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1746393
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