A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10024



Internal ID15196087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73528977..73560021hg38UCSC Ensembl
Outerchr14:73995681..74026725hg19UCSC Ensembl
Outerchr14:73065434..73096478hg18UCSC Ensembl
Outerchr14:73065434..73096478hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3831045
hg1931045
hg1831045
hg1731045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1350
Supporting Variants
SamplesNA18956
Known GenesACOT1, HEATR4
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)nssv10024
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