A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733



Internal ID15549472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:15609106..15641537hg38UCSC Ensembl
Outerchr5:15609215..15641646hg19UCSC Ensembl
Outerchr5:15662215..15694646hg18UCSC Ensembl
Outerchr5:15662215..15694646hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg387071
hg197071
hg187071
hg177071
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10438
SamplesNA18956
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)nsv4733
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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