A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20629



Internal ID15490287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70118898..70162024hg38UCSC Ensembl
Outerchr16:70118267..70162818hg38UCSC Ensembl
Innerchr16:70152801..70195927hg19UCSC Ensembl
Outerchr16:70152170..70196721hg19UCSC Ensembl
Innerchr16:68710302..68753428hg18UCSC Ensembl
Outerchr16:68709671..68754222hg18UCSC Ensembl
Innerchr16:68710302..68753428hg17UCSC Ensembl
Outerchr16:68709671..68754222hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3844552
hg1944552
hg1844552
hg1744552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA18572
Known GenesPDPR
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)nssv20629
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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