A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19259



Internal ID15843155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46748547..46772071hg38UCSC Ensembl
Outerchr10:46748035..46772551hg38UCSC Ensembl
Innerchr10:46777556..46801063hg19UCSC Ensembl
Outerchr10:46777076..46801575hg19UCSC Ensembl
Innerchr10:46197562..46221069hg18UCSC Ensembl
Outerchr10:46197082..46221581hg18UCSC Ensembl
Innerchr10:46197562..46221069hg17UCSC Ensembl
Outerchr10:46197082..46221581hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3824517
hg1924500
hg1824500
hg1724500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19173
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)nssv19259
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