A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18836



Internal ID15494731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45951449..45951492hg38UCSC Ensembl
Outerchr10:45950893..45951841hg38UCSC Ensembl
Innerchr10:51350365..51350408hg19UCSC Ensembl
Outerchr10:51349809..51350757hg19UCSC Ensembl
Innerchr10:51020371..51020414hg18UCSC Ensembl
Outerchr10:51019815..51020763hg18UCSC Ensembl
Innerchr10:51020371..51020414hg17UCSC Ensembl
Outerchr10:51019815..51020763hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38949
hg19949
hg18949
hg17949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8648
Supporting Variants
SamplesNA19007
Known GenesLOC728407, PARG
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)nssv18836
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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