A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1367



Internal ID15545930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:78601178..78640044hg38UCSC Ensembl
Outerchr14:79067521..79106387hg19UCSC Ensembl
Outerchr14:78137274..78176140hg18UCSC Ensembl
Outerchr14:78137274..78176140hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3838867
hg1938867
hg1838867
hg1738867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9222
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)nsv1367
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