A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26626



Internal ID15842546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10570428..10649273hg38UCSC Ensembl
Outerchr21:10559000..10660645hg38UCSC Ensembl
Innerchr21:10863184..10942029hg19UCSC Ensembl
Outerchr21:10851812..10953457hg19UCSC Ensembl
Innerchr21:9885055..9963900hg18UCSC Ensembl
Outerchr21:9873683..9975328hg18UCSC Ensembl
Innerchr21:9885055..9963900hg17UCSC Ensembl
Outerchr21:9873683..9975328hg17UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38101646
hg19101646
hg18101646
hg17101646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9837
Supporting Variants
SamplesNA19144
Known GenesTPTE
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)nssv26626
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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