A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24245



Internal ID15844065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57960273..57962417hg38UCSC Ensembl
Outerchr10:57959752..57963264hg38UCSC Ensembl
Innerchr10:59720033..59722177hg19UCSC Ensembl
Outerchr10:59719512..59723024hg19UCSC Ensembl
Innerchr10:59390039..59392183hg18UCSC Ensembl
Outerchr10:59389518..59393030hg18UCSC Ensembl
Innerchr10:59390039..59392183hg17UCSC Ensembl
Outerchr10:59389518..59393030hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383513
hg193513
hg183513
hg173513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8677
Supporting Variants
SamplesNA19221
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)nssv24245
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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