A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20611



Internal ID15844680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46748547..46753055hg38UCSC Ensembl
Outerchr10:46748035..46753738hg38UCSC Ensembl
Innerchr10:46796551..46801063hg19UCSC Ensembl
Outerchr10:46795865..46801575hg19UCSC Ensembl
Innerchr10:46216557..46221069hg18UCSC Ensembl
Outerchr10:46215871..46221581hg18UCSC Ensembl
Innerchr10:46216557..46221069hg17UCSC Ensembl
Outerchr10:46215871..46221581hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385704
hg195711
hg185711
hg175711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19240
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)nssv20611
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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