A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18834



Internal ID15840031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122600525..122616794hg38UCSC Ensembl
Outerchr10:122599796..122617670hg38UCSC Ensembl
Innerchr10:124360041..124376310hg19UCSC Ensembl
Outerchr10:124359312..124377186hg19UCSC Ensembl
Innerchr10:124350031..124366300hg18UCSC Ensembl
Outerchr10:124349302..124367176hg18UCSC Ensembl
Innerchr10:124350031..124366300hg17UCSC Ensembl
Outerchr10:124349302..124367176hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817875
hg1917875
hg1817875
hg1717875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8731
Supporting Variants
SamplesNA18975
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)nssv18834
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