A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8369



Internal ID15846281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150023059..150024730hg38UCSC Ensembl
Outerchr1:149995017..149996688hg19UCSC Ensembl
Outerchr1:148261641..148263312hg18UCSC Ensembl
Outerchr1:146808090..146809761hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381672
hg191672
hg181672
hg171672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21762, nssv25450, nssv20737, nssv20757, nssv19105, nssv21753, nssv23368, nssv25185, nssv19419
SamplesNA18502, NA11830, NA18980, NA07029, NA07048, NA19132, NA18517, NA12740, NA19173
Known Genes
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)nsv8369
Frequency
Sample Size31
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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