A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4296



Internal ID15548991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34952357..34986325hg38UCSC Ensembl
Outerchr4:34953979..34987947hg19UCSC Ensembl
Outerchr4:34630374..34664342hg18UCSC Ensembl
Outerchr4:34776545..34810513hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386059
hg196059
hg186059
hg176059
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3126
SamplesNA18555
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)nsv4296
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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