A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6652



Internal ID15190526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:843912..850205hg38UCSC Ensembl
Outerchr16:893912..900205hg19UCSC Ensembl
Outerchr16:833913..840206hg18UCSC Ensembl
Outerchr16:833913..840206hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389831
hg199831
hg189831
hg179831
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1704
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)nssv6652
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