A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088948



Internal ID21274009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28293748..28312758hg38UCSC Ensembl
Innerchr10:28582677..28601687hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3819011
hg1919011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111277
Supporting Variants
Samplessample20
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088948
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