A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23923



Internal ID15844111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48045424..48049522hg38UCSC Ensembl
Outerchr10:48045060..48049695hg38UCSC Ensembl
Innerchr10:49253446..49257544hg19UCSC Ensembl
Outerchr10:49253082..49257717hg19UCSC Ensembl
Innerchr10:48923452..48927550hg18UCSC Ensembl
Outerchr10:48923088..48927723hg18UCSC Ensembl
Innerchr10:48923452..48927550hg17UCSC Ensembl
Outerchr10:48923088..48927723hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384636
hg194636
hg184636
hg174636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
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)nssv23923
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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