A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3493



Internal ID15548108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:32134383..32179517hg38UCSC Ensembl
Outerchr21:33506694..33551829hg19UCSC Ensembl
Outerchr21:32428565..32473700hg18UCSC Ensembl
Outerchr21:32428565..32473700hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3845135
hg1945136
hg1845136
hg1745136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5899
SamplesNA19129
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)nsv3493
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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