A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437



Internal ID15549146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:98765457..98798975hg38UCSC Ensembl
Outerchr4:99686608..99720126hg19UCSC Ensembl
Outerchr4:99905631..99939149hg18UCSC Ensembl
Outerchr4:100043786..100077304hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385768
hg195768
hg185768
hg175768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4770
SamplesNA19129
Known Genes
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)nsv4437
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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