A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5910



Internal ID15196784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45076500..45116714hg38UCSC Ensembl
Outerchr21:46496415..46536629hg19UCSC Ensembl
Outerchr21:45320843..45361057hg18UCSC Ensembl
Outerchr21:45320843..45361057hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3840215
hg1940215
hg1840215
hg1740215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3541
Supporting Variants
SamplesNA19129
Known GenesADARB1
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)nssv5910
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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