A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103202



Internal ID21291440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:224952936..224959923hg38UCSC Ensembl
Innerchr2:225817653..225824640hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg386988
hg196988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114859
Supporting Variants
Samplessample73
Known GenesDOCK10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103202
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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