A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089031



Internal ID21290666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51328090..51334641hg38UCSC Ensembl
Innerchr10:53087850..53094401hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg386552
hg196552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113837
Supporting Variants
Samplessample62
Known GenesPRKG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089031
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