A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25934



Internal ID15492996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21739770..21797844hg38UCSC Ensembl
Outerchr16:21739346..21798399hg38UCSC Ensembl
Innerchr16:21751091..21809165hg19UCSC Ensembl
Outerchr16:21750667..21809720hg19UCSC Ensembl
Innerchr16:21658592..21716666hg18UCSC Ensembl
Outerchr16:21658168..21717221hg18UCSC Ensembl
Innerchr16:21658592..21716666hg17UCSC Ensembl
Outerchr16:21658168..21717221hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3859054
hg1959054
hg1859054
hg1759054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9397
Supporting Variants
SamplesNA18972
Known GenesOTOA, RRN3P1
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)nssv25934
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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