A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21792



Internal ID15833101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122584215..122585858hg38UCSC Ensembl
Outerchr10:122582945..122586075hg38UCSC Ensembl
Innerchr10:124343731..124345374hg19UCSC Ensembl
Outerchr10:124342461..124345591hg19UCSC Ensembl
Innerchr10:124333721..124335364hg18UCSC Ensembl
Outerchr10:124332451..124335581hg18UCSC Ensembl
Innerchr10:124333721..124335364hg17UCSC Ensembl
Outerchr10:124332451..124335581hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383131
hg193131
hg183131
hg173131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8731
Supporting Variants
SamplesNA18502
Known GenesDMBT1
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)nssv21792
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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