A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096863



Internal ID21269407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89632082..89635804hg38UCSC Ensembl
Innerchr1:90097641..90101363hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg383723
hg193723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115332
Supporting Variants
Samplessample138
Known GenesFLJ27354, LRRC8C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096863
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