A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6638



Internal ID15551567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99548730..99583267hg38UCSC Ensembl
Outerchr9:102311012..102345549hg19UCSC Ensembl
Outerchr9:101350833..101385370hg18UCSC Ensembl
Outerchr9:99390567..99425104hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385474
hg195474
hg185474
hg175474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2817
SamplesNA18555
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)nsv6638
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