A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20961



Internal ID15491928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68431715..68454875hg38UCSC Ensembl
Outerchr9:68427991..68514936hg38UCSC Ensembl
Innerchr9:71046631..71069791hg19UCSC Ensembl
Outerchr9:71042907..71129852hg19UCSC Ensembl
Innerchr9:70236451..70259611hg18UCSC Ensembl
Outerchr9:70232727..70319672hg18UCSC Ensembl
Innerchr9:68276185..68299345hg17UCSC Ensembl
Outerchr9:68272461..68359406hg17UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3886946
hg1986946
hg1886946
hg1786946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8521
Supporting Variants
SamplesNA18860
Known GenesPGM5
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)nssv20961
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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