A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3586



Internal ID15548210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:27810628..27843037hg38UCSC Ensembl
Outerchr22:28206616..28239025hg19UCSC Ensembl
Outerchr22:26536616..26569025hg18UCSC Ensembl
Outerchr22:26531170..26563579hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg387302
hg197302
hg187302
hg177302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4581
SamplesNA12878
Known GenesMIR548AM
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)nsv3586
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