A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6668



Internal ID15204914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112371097..112405645hg38UCSC Ensembl
Outerchr9:115133377..115167925hg19UCSC Ensembl
Outerchr9:114173198..114207746hg18UCSC Ensembl
Outerchr9:112212932..112247480hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385464
hg195464
hg185464
hg175464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2820
SamplesNA18555
Known GenesHSDL2
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)nsv6668
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