A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23760



Internal ID15843024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25740969..25741936hg38UCSC Ensembl
Outerchr16:25740399..25742901hg38UCSC Ensembl
Innerchr16:25752290..25753257hg19UCSC Ensembl
Outerchr16:25751720..25754222hg19UCSC Ensembl
Innerchr16:25659791..25660758hg18UCSC Ensembl
Outerchr16:25659221..25661723hg18UCSC Ensembl
Innerchr16:25659791..25660758hg17UCSC Ensembl
Outerchr16:25659221..25661723hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382503
hg192503
hg182503
hg172503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9407
Supporting Variants
SamplesNA19173
Known GenesHS3ST4
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)nssv23760
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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