A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3452



Internal ID15548063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:13845848..13905135hg38UCSC Ensembl
Outerchr21:15218169..15277456hg19UCSC Ensembl
Outerchr21:14140040..14199327hg18UCSC Ensembl
Outerchr21:14140040..14199327hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3859288
hg1959288
hg1859288
hg1759288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9601, nssv1616
SamplesNA18507, NA19240
Known GenesC21orf15
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)nsv3452
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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