A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18626



Internal ID15841440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48010002..48018513hg38UCSC Ensembl
Outerchr10:48008423..48018615hg38UCSC Ensembl
Innerchr10:49218027..49226529hg19UCSC Ensembl
Outerchr10:49216447..49226631hg19UCSC Ensembl
Innerchr10:48888033..48896535hg18UCSC Ensembl
Outerchr10:48886453..48896637hg18UCSC Ensembl
Innerchr10:48888033..48896535hg17UCSC Ensembl
Outerchr10:48886453..48896637hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810193
hg1910185
hg1810185
hg1710185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19007
Known GenesCTGLF12P
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)nssv18626
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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