A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4362



Internal ID15549064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:64713483..64734383hg38UCSC Ensembl
Outerchr4:65579201..65600101hg19UCSC Ensembl
Outerchr4:65261796..65282696hg18UCSC Ensembl
Outerchr4:65407967..65428867hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg386310
hg196310
hg186310
hg176310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3129
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)nsv4362
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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