A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135372



Internal ID18936381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:89567499..89567598hg38UCSC Ensembl
Outerchr14:90033843..90033942hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1121n106
Supporting Variantsnssv3988932
SamplesKWS1
Known GenesFOXN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135372
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