A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18945



Internal ID15834629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47623331..47624897hg38UCSC Ensembl
Outerchr10:47623020..47625622hg38UCSC Ensembl
Innerchr10:47313349..47314919hg19UCSC Ensembl
Outerchr10:47313038..47315642hg19UCSC Ensembl
Innerchr10:46733355..46734925hg18UCSC Ensembl
Outerchr10:46733044..46735648hg18UCSC Ensembl
Innerchr10:46733355..46734925hg17UCSC Ensembl
Outerchr10:46733044..46735648hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382603
hg192605
hg182605
hg172605
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)nssv18945
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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