A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375



Internal ID15829223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46843556..46862128hg38UCSC Ensembl
Outerchr10:46843083..46868354hg38UCSC Ensembl
Innerchr10:48877234..48895806hg19UCSC Ensembl
Outerchr10:48871008..48896279hg19UCSC Ensembl
Innerchr10:48497240..48515812hg18UCSC Ensembl
Outerchr10:48491014..48516285hg18UCSC Ensembl
Innerchr10:48497240..48515812hg17UCSC Ensembl
Outerchr10:48491014..48516285hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825272
hg1925272
hg1825272
hg1725272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA10847
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)nssv17375
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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