A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4450



Internal ID15202475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106116666..106161512hg38UCSC Ensembl
Outerchr4:107037823..107082669hg19UCSC Ensembl
Outerchr4:107257272..107302118hg18UCSC Ensembl
Outerchr4:107395427..107440273hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3844847
hg1944847
hg1844847
hg1744847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7111, nssv4773
SamplesNA12156, NA19129
Known GenesTBCK
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)nsv4450
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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