A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009413



Internal ID22071044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22453246..22514241hg38UCSC Ensembl
Outerchr14:22448641..22519044hg38UCSC Ensembl
Innerchr14:22922238..22983223hg19UCSC Ensembl
Outerchr14:22917633..22988022hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3870404
hg1970390
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155011
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009413
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