A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4134



Internal ID15538861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105671362..105861206hg38UCSC Ensembl
Outerchr14:106137699..106327416hg19UCSC Ensembl
Outerchr14:105208744..105398461hg18UCSC Ensembl
Outerchr14:105208744..105398461hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38189845
hg19189718
hg18189718
hg17189718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA12878
Known GenesELK2AP
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)nssv4134
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