A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1366



Internal ID15199243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:78166701..78211375hg38UCSC Ensembl
Outerchr14:78633044..78677718hg19UCSC Ensembl
Outerchr14:77702797..77747471hg18UCSC Ensembl
Outerchr14:77702797..77747471hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3844675
hg1944675
hg1844675
hg1744675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9221
SamplesNA12156
Known GenesNRXN3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1366
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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