A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19997



Internal ID15836177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122579593..122595648hg38UCSC Ensembl
Outerchr10:122579399..122596918hg38UCSC Ensembl
Innerchr10:124339109..124355164hg19UCSC Ensembl
Outerchr10:124338915..124356434hg19UCSC Ensembl
Innerchr10:124329099..124345154hg18UCSC Ensembl
Outerchr10:124328905..124346424hg18UCSC Ensembl
Innerchr10:124329099..124345154hg17UCSC Ensembl
Outerchr10:124328905..124346424hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817520
hg1917520
hg1817520
hg1717520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8731
Supporting Variants
SamplesNA18563
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)nssv19997
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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