A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4550



Internal ID15539277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:14434471..14440110hg38UCSC Ensembl
Outerchr21:15806792..15812431hg19UCSC Ensembl
Outerchr21:14728663..14734302hg18UCSC Ensembl
Outerchr21:14728663..14734302hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3812090
hg1912090
hg1812090
hg1712090
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3456
Supporting Variants
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)nssv4550
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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