A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105195



Internal ID21278533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5293491..5312902hg38UCSC Ensembl
Innerchr2:5433624..5453035hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3819412
hg1919412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114580
Supporting Variants
Samplessample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105195
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