A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7013



Internal ID15536851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:75399147..75418648hg38UCSC Ensembl
Outerchr3:75448298..75467799hg19UCSC Ensembl
Outerchr3:75530988..75550489hg18UCSC Ensembl
Outerchr3:75530988..75550489hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3811729
hg1911729
hg1811729
hg1711729
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3883
Supporting Variants
SamplesNA12156
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)nssv7013
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer