A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18926



Internal ID15494722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45876167..45914176hg38UCSC Ensembl
Outerchr10:45876167..45915679hg38UCSC Ensembl
Innerchr10:51681650..51722311hg19UCSC Ensembl
Outerchr10:51680147..51722579hg19UCSC Ensembl
Innerchr10:51351656..51392317hg18UCSC Ensembl
Outerchr10:51350153..51392585hg18UCSC Ensembl
Innerchr10:51351656..51392317hg17UCSC Ensembl
Outerchr10:51350153..51392585hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3839513
hg1942433
hg1842433
hg1742433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8654
Supporting Variants
SamplesNA19007
Known Genes
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)nssv18926
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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