A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2092



Internal ID15541375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:106320908..106375020hg38UCSC Ensembl
Outerchr14:106777165..106830951hg19UCSC Ensembl
Outerchr14:105848210..105901996hg18UCSC Ensembl
Outerchr14:105848210..105901996hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3854113
hg1953787
hg1853787
hg1753787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA18555
Known Genes
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)nssv2092
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