A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9776



Internal ID15847688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1581888..1604127hg38UCSC Ensembl
Outerchr20:1562534..1584773hg19UCSC Ensembl
Outerchr20:1510534..1532773hg18UCSC Ensembl
Outerchr20:1510534..1532773hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822240
hg1922240
hg1822240
hg1722240
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22579, nssv24994, nssv24080, nssv26069, nssv25200, nssv27666, nssv24745, nssv25564, nssv27887, nssv24728, nssv21875, nssv24540, nssv27660, nssv28605, nssv24247, nssv25908, nssv26834, nssv26429, nssv25555, nssv25426, nssv27098
SamplesNA18502, NA11830, NA07029, NA12155, NA18563, NA18860, NA18942, NA07048, NA18975, NA19007, NA10847, NA10863, NA18572, NA19221, NA18537, NA18517, NA18564, NA19240, NA19144, NA19173, NA18552
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)nsv9776
Frequency
Sample Size31
Observed Gain4
Observed Loss17
Observed Complex0
Frequencyn/a


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