A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4819



Internal ID15196415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:15524058..15555042hg38UCSC Ensembl
Outerchr5:15524167..15555151hg19UCSC Ensembl
Outerchr5:15577167..15608151hg18UCSC Ensembl
Outerchr5:15577167..15608151hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg388269
hg198269
hg188269
hg178269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730
Supporting Variants
SamplesNA19129
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)nssv4819
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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