A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734



Internal ID15549473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:15727957..15761083hg38UCSC Ensembl
Outerchr5:15728066..15761192hg19UCSC Ensembl
Outerchr5:15781066..15814192hg18UCSC Ensembl
Outerchr5:15781066..15814192hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386850
hg196850
hg186850
hg176850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2507
SamplesNA18555
Known GenesFBXL7
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)nsv4734
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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