A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1727322



Internal ID12543754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66760434..66761087hg38UCSC Ensembl
chr16:66794337..66794990hg19UCSC Ensembl
chr16:65351838..65352491hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38654
hg19654
hg18654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3629774
SamplesHuRef
Known GenesCCDC79
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1727322
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