A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4451



Internal ID15549162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106678800..106692224hg38UCSC Ensembl
Outerchr4:107599957..107613381hg19UCSC Ensembl
Outerchr4:107819406..107832830hg18UCSC Ensembl
Outerchr4:107957561..107970985hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813425
hg1913425
hg1813425
hg1713425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3273
SamplesNA12878
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)nsv4451
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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