A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8640



Internal ID15535224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98449035..98482700hg38UCSC Ensembl
Outerchr9:101211317..101244982hg19UCSC Ensembl
Outerchr9:100251138..100284803hg18UCSC Ensembl
Outerchr9:98290872..98324537hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385774
hg195774
hg185774
hg175774
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6629
Supporting Variants
SamplesNA12156
Known GenesGABBR2
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)nssv8640
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