A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8697



Internal ID15499923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79710063..79746090hg38UCSC Ensembl
Outerchr10:81469819..81505846hg19UCSC Ensembl
Outerchr10:81139825..81175852hg18UCSC Ensembl
Outerchr10:81139825..81175852hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3836028
hg1936028
hg1836028
hg1736028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22403, nssv17599, nssv19066, nssv20198, nssv19727, nssv24405, nssv18534, nssv19324
SamplesNA18975, NA10839, NA18972, NA12155, NA18563, NA18572, NA19221, NA18552
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)nsv8697
Frequency
Sample Size31
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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