A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4558



Internal ID15549279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:153929374..153962637hg38UCSC Ensembl
Outerchr4:154850526..154883789hg19UCSC Ensembl
Outerchr4:155069976..155103239hg18UCSC Ensembl
Outerchr4:155208131..155241394hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg386176
hg196176
hg186176
hg176176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8015
SamplesNA12156
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)nsv4558
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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