A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv537



Internal ID15203486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126216495..126245751hg38UCSC Ensembl
Outerchr11:126086390..126115646hg19UCSC Ensembl
Outerchr11:125591600..125620856hg18UCSC Ensembl
Outerchr11:125591600..125620856hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3811746
hg1911746
hg1811746
hg1711746
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1050
SamplesNA19240
Known GenesFAM118B
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)nsv537
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