A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4026



Internal ID15548694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136504142..136535954hg38UCSC Ensembl
Outerchr3:136222984..136254796hg19UCSC Ensembl
Outerchr3:137705674..137737486hg18UCSC Ensembl
Outerchr3:137705682..137737494hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg387686
hg197686
hg187686
hg177686
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10364
SamplesNA18956
Known GenesSTAG1
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)nsv4026
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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