A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4453



Internal ID15202478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106904437..106934973hg38UCSC Ensembl
Outerchr4:107825594..107856130hg19UCSC Ensembl
Outerchr4:108045043..108075579hg18UCSC Ensembl
Outerchr4:108183198..108213734hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3810433
hg1910433
hg1810433
hg1710433
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv404
SamplesNA19240
Known GenesDKK2
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)nsv4453
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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