A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3867



Internal ID15191908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:17435188..17469309hg38UCSC Ensembl
Outerchr10:17477187..17511308hg19UCSC Ensembl
Outerchr10:17517193..17551314hg18UCSC Ensembl
Outerchr10:17517193..17551314hg17UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385626
hg195626
hg185626
hg175626
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966
Supporting Variants
SamplesNA12878
Known GenesST8SIA6
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)nssv3867
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