A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24959



Internal ID15481282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10458586..10491316hg38UCSC Ensembl
Outerchr21:10458059..10491745hg38UCSC Ensembl
Innerchr21:11021141..11053871hg19UCSC Ensembl
Outerchr21:11020712..11054398hg19UCSC Ensembl
Innerchr21:10043012..10075742hg18UCSC Ensembl
Outerchr21:10042583..10076269hg18UCSC Ensembl
Innerchr21:10043012..10075742hg17UCSC Ensembl
Outerchr21:10042583..10076269hg17UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3833687
hg1933687
hg1833687
hg1733687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9838
Supporting Variants
SamplesNA07048
Known GenesBAGE2, BAGE3, BAGE4, BAGE5
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv24959
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer