A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9612



Internal ID15539702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36522149..36544648hg38UCSC Ensembl
Outerchr22:36918196..36940695hg19UCSC Ensembl
Outerchr22:35248142..35270641hg18UCSC Ensembl
Outerchr22:35242696..35265195hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3814196
hg1914196
hg1814196
hg1714196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3615
Supporting Variants
SamplesNA18507
Known GenesEIF3D
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)nssv9612
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