A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20872



Internal ID15492194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14694958..14707766hg38UCSC Ensembl
Outerchr16:14694480..14709220hg38UCSC Ensembl
Innerchr16:14788815..14801623hg19UCSC Ensembl
Outerchr16:14788337..14803077hg19UCSC Ensembl
Innerchr16:14696316..14709124hg18UCSC Ensembl
Outerchr16:14695838..14710578hg18UCSC Ensembl
Innerchr16:14696316..14709124hg17UCSC Ensembl
Outerchr16:14695838..14710578hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3814741
hg1914741
hg1814741
hg1714741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9353
Supporting Variants
SamplesNA18942
Known GenesPLA2G10
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)nssv20872
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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