A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5956



Internal ID15543415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:38213532..38216759hg38UCSC Ensembl
Outerchr3:38255023..38258250hg19UCSC Ensembl
Outerchr3:38230027..38233254hg18UCSC Ensembl
Outerchr3:38230027..38233254hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385786
hg195786
hg185786
hg175786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3768
Supporting Variants
SamplesNA19129
Known GenesOXSR1
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)nssv5956
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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