A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18915



Internal ID15834599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46378985..46396020hg38UCSC Ensembl
Outerchr10:46378639..46396571hg38UCSC Ensembl
Innerchr10:47153742..47170777hg19UCSC Ensembl
Outerchr10:47153191..47171131hg19UCSC Ensembl
Innerchr10:46573748..46590783hg18UCSC Ensembl
Outerchr10:46573197..46591137hg18UCSC Ensembl
Innerchr10:46573748..46590783hg17UCSC Ensembl
Outerchr10:46573197..46591137hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817933
hg1917941
hg1817941
hg1717941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18537
Known GenesANXA8
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)nssv18915
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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