A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5953



Internal ID15196732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32993465..33027225hg38UCSC Ensembl
Outerchr3:33034957..33068717hg19UCSC Ensembl
Outerchr3:33009961..33043721hg18UCSC Ensembl
Outerchr3:33009961..33043721hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385517
hg195517
hg185517
hg175517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3753
Supporting Variants
SamplesNA19129
Known GenesGLB1
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)nssv5953
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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