A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10830



Internal ID15541968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:77787954..77820182hg38UCSC Ensembl
Outerchr11:77499000..77531228hg19UCSC Ensembl
Outerchr11:77176648..77208876hg18UCSC Ensembl
Outerchr11:77176648..77208876hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg387277
hg197277
hg187277
hg177277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv398
Supporting Variants
SamplesNA18956
Known GenesRSF1
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)nssv10830
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