A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105143



Internal ID21277664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67101757..67131378hg38UCSC Ensembl
Innerchr2:67328889..67358510hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3829622
hg1929622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117036
Supporting Variants
Samplessample256
Known GenesLOC644838
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105143
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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