A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8617



Internal ID15846529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37526873..37588403hg38UCSC Ensembl
Outerchr10:37815801..37877331hg19UCSC Ensembl
Outerchr10:37855807..37917337hg18UCSC Ensembl
Outerchr10:37855807..37917337hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3861531
hg1961531
hg1861531
hg1761531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23424, nssv21614
SamplesNA19221, NA18517
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)nsv8617
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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