A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1837



Internal ID15546400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:66328158..66361916hg38UCSC Ensembl
Outerchr16:66362061..66395819hg19UCSC Ensembl
Outerchr16:64919562..64953320hg18UCSC Ensembl
Outerchr16:64919562..64953320hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385978
hg195978
hg185978
hg175978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4218
SamplesNA12878
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)nsv1837
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