A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20684



Internal ID15834484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:515991..526633hg38UCSC Ensembl
Outerchr9:514417..530198hg38UCSC Ensembl
Innerchr9:515991..526633hg19UCSC Ensembl
Outerchr9:514417..530198hg19UCSC Ensembl
Innerchr9:505991..516633hg18UCSC Ensembl
Outerchr9:504417..520198hg18UCSC Ensembl
Innerchr9:505991..516633hg17UCSC Ensembl
Outerchr9:504417..520198hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3815782
hg1915782
hg1815782
hg1715782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8404
Supporting Variants
SamplesNA18517
Known GenesKANK1
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)nssv20684
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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