A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3615



Internal ID15548242
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 StatusM
Merged Variants
Supporting Variantsnssv9612
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)nsv3615
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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