A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118185



Internal ID21301451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36441142..36442464hg38UCSC Ensembl
Innerchr2:36668285..36669607hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102531
Samplessample64
Known GenesCRIM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118185
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