A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18896



Internal ID15494724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45928990..45929027hg38UCSC Ensembl
Outerchr10:45928399..45929596hg38UCSC Ensembl
Innerchr10:51666800..51666837hg19UCSC Ensembl
Outerchr10:51666231..51667428hg19UCSC Ensembl
Innerchr10:51336806..51336843hg18UCSC Ensembl
Outerchr10:51336237..51337434hg18UCSC Ensembl
Innerchr10:51336806..51336843hg17UCSC Ensembl
Outerchr10:51336237..51337434hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
hg171198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8653
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)nssv18896
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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