A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3797



Internal ID15201756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45852130..45886233hg38UCSC Ensembl
Outerchr3:45893622..45927725hg19UCSC Ensembl
Outerchr3:45868626..45902729hg18UCSC Ensembl
Outerchr3:45868626..45902729hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg386880
hg196880
hg186880
hg176880
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673
SamplesNA19240
Known GenesLZTFL1
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)nsv3797
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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