A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19316



Internal ID15494682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133657627..133659364hg38UCSC Ensembl
Outerchr10:133656542..133660020hg38UCSC Ensembl
Innerchr10:135471131..135472868hg19UCSC Ensembl
Outerchr10:135470046..135473524hg19UCSC Ensembl
Innerchr10:135321121..135322858hg18UCSC Ensembl
Outerchr10:135320036..135323514hg18UCSC Ensembl
Innerchr10:135360012..135361749hg17UCSC Ensembl
Outerchr10:135358927..135362405hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383479
hg193479
hg183479
hg173479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8752
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)nssv19316
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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