A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735



Internal ID15549474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:15916237..15961323hg38UCSC Ensembl
Outerchr5:15916346..15961432hg19UCSC Ensembl
Outerchr5:15969346..16014432hg18UCSC Ensembl
Outerchr5:15969346..16014432hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3845087
hg1945087
hg1845087
hg1745087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8073
SamplesNA12156
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)nsv4735
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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