A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4283



Internal ID15548977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:29215379..29241484hg38UCSC Ensembl
Outerchr4:29217001..29243106hg19UCSC Ensembl
Outerchr4:28826099..28852204hg18UCSC Ensembl
Outerchr4:28893270..28919375hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3826106
hg1926106
hg1826106
hg1726106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv380
SamplesNA19240
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)nsv4283
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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