A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24626



Internal ID15829489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1604738..1614942hg38UCSC Ensembl
Outerchr20:1604127..1615887hg38UCSC Ensembl
Innerchr20:1585384..1595588hg19UCSC Ensembl
Outerchr20:1584773..1596533hg19UCSC Ensembl
Innerchr20:1533384..1543588hg18UCSC Ensembl
Outerchr20:1532773..1544533hg18UCSC Ensembl
Innerchr20:1533384..1543588hg17UCSC Ensembl
Outerchr20:1532773..1544533hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811761
hg1911761
hg1811761
hg1711761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9777
Supporting Variants
SamplesNA10863
Known GenesSIRPB1
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)nssv24626
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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