A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9201



Internal ID15534663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:60412426..60457483hg38UCSC Ensembl
Outerchr14:60879144..60924201hg19UCSC Ensembl
Outerchr14:59948897..59993954hg18UCSC Ensembl
Outerchr14:59948897..59993954hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3845058
hg1945058
hg1845058
hg1745058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1294
Supporting Variants
SamplesNA12156
Known GenesC14orf39
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)nssv9201
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