A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981299



Internal ID18877633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:89360656..89362856hg38UCSC Ensembl
Outerchr14:89827000..89829200hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143615
Supporting Variants
SamplesKWS1
Known GenesFOXN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981299
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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