A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8639



Internal ID15535225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98078387..98112075hg38UCSC Ensembl
Outerchr9:100840669..100874357hg19UCSC Ensembl
Outerchr9:99880490..99914178hg18UCSC Ensembl
Outerchr9:97920224..97953912hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385750
hg195750
hg185750
hg175750
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6628
Supporting Variants
SamplesNA12156
Known GenesNANS, TRIM14
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)nssv8639
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