A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19065



Internal ID15834749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46840043..46841978hg38UCSC Ensembl
Innerchr10:48897384..48899319hg19UCSC Ensembl
Outerchr10:48896279..48901259hg19UCSC Ensembl
Innerchr10:48517390..48519325hg18UCSC Ensembl
Outerchr10:48516285..48521265hg18UCSC Ensembl
Innerchr10:48517390..48519325hg17UCSC Ensembl
Outerchr10:48516285..48521265hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381936
hg194981
hg184981
hg174981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18537
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)nssv19065
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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