A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22403



Internal ID15492863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79710219..79732633hg38UCSC Ensembl
Outerchr10:79710063..79733161hg38UCSC Ensembl
Innerchr10:81469975..81492389hg19UCSC Ensembl
Outerchr10:81469819..81492917hg19UCSC Ensembl
Innerchr10:81139981..81162395hg18UCSC Ensembl
Outerchr10:81139825..81162923hg18UCSC Ensembl
Innerchr10:81139981..81162395hg17UCSC Ensembl
Outerchr10:81139825..81162923hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3823099
hg1923099
hg1823099
hg1723099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8697
Supporting Variants
SamplesNA18972
Known GenesNUTM2B
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)nssv22403
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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