A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20368



Internal ID15842384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47574469..47574499hg38UCSC Ensembl
Outerchr10:47573852..47574814hg38UCSC Ensembl
Innerchr10:48973407..48973437hg19UCSC Ensembl
Outerchr10:48972788..48973752hg19UCSC Ensembl
Innerchr10:48593413..48593443hg18UCSC Ensembl
Outerchr10:48592794..48593758hg18UCSC Ensembl
Innerchr10:48593413..48593443hg17UCSC Ensembl
Outerchr10:48592794..48593758hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38963
hg19965
hg18965
hg17965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19144
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)nssv20368
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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