A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8677



Internal ID15846589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:57811017..58012038hg38UCSC Ensembl
Outerchr10:59570777..59771798hg19UCSC Ensembl
Outerchr10:59240783..59441804hg18UCSC Ensembl
Outerchr10:59240783..59441804hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38201022
hg19201022
hg18201022
hg17201022
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19305, nssv19294, nssv24245, nssv17479
SamplesNA10839, NA18572, NA19221, NA18537
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)nsv8677
Frequency
Sample Size31
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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