A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8151



Internal ID15535713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133565926..133600016hg38UCSC Ensembl
Outerchr5:132901617..132935707hg19UCSC Ensembl
Outerchr5:132929516..132963606hg18UCSC Ensembl
Outerchr5:132929516..132963606hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg385345
hg195345
hg185345
hg175345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5007
Supporting Variants
SamplesNA12156
Known GenesFSTL4
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)nssv8151
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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