A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26155



Internal ID15835097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63964818..63965874hg38UCSC Ensembl
Outerchr20:63964349..63966961hg38UCSC Ensembl
Innerchr20:62596171..62597227hg19UCSC Ensembl
Outerchr20:62595702..62598314hg19UCSC Ensembl
Innerchr20:62066615..62067671hg18UCSC Ensembl
Outerchr20:62066146..62068758hg18UCSC Ensembl
Innerchr20:62066615..62067671hg17UCSC Ensembl
Outerchr20:62066146..62068758hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382613
hg192613
hg182613
hg172613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9830
Supporting Variants
SamplesNA18537
Known GenesZNF512B
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)nssv26155
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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