A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155040



Internal ID22085545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93140066..93149262hg38UCSC Ensembl
Outerchr14:93139233..93149575hg38UCSC Ensembl
Innerchr14:93606411..93615607hg19UCSC Ensembl
Outerchr14:93605578..93615920hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3810343
hg1910343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009710, nssv4009709
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155040
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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