A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4790



Internal ID15196464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:153163194..153197065hg38UCSC Ensembl
Outerchr4:154084346..154118217hg19UCSC Ensembl
Outerchr4:154303796..154337667hg18UCSC Ensembl
Outerchr4:154441951..154475822hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385416
hg195416
hg185416
hg175416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4556
Supporting Variants
SamplesNA19129
Known GenesTRIM2
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)nssv4790
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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