A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964



Internal ID15538691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:73493154..73528478hg38UCSC Ensembl
Outerchr11:73204199..73239523hg19UCSC Ensembl
Outerchr11:72881847..72917171hg18UCSC Ensembl
Outerchr11:72881847..72917171hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384414
hg194414
hg184414
hg174414
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv389
Supporting Variants
SamplesNA12878
Known GenesFAM168A
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)nssv3964
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