A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009708



Internal ID22071339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86871554..86876637hg38UCSC Ensembl
Outerchr14:86867666..86877815hg38UCSC Ensembl
Innerchr14:87337898..87342981hg19UCSC Ensembl
Outerchr14:87334010..87344159hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3810150
hg1910150
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155039
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009708
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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