A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3499



Internal ID15548114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:34121679..34166971hg38UCSC Ensembl
Outerchr21:35493978..35539271hg19UCSC Ensembl
Outerchr21:34415848..34461141hg18UCSC Ensembl
Outerchr21:34415848..34461141hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3845293
hg1945294
hg1845294
hg1745294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7717
SamplesNA12156
Known GenesMRPS6
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)nsv3499
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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