A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24325



Internal ID15495564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32687902..32687905hg38UCSC Ensembl
Outerchr16:32687839..32688779hg38UCSC Ensembl
Innerchr16:32699223..32699226hg19UCSC Ensembl
Outerchr16:32699160..32700100hg19UCSC Ensembl
Innerchr16:32606724..32606727hg18UCSC Ensembl
Outerchr16:32606661..32607601hg18UCSC Ensembl
Innerchr16:32606724..32606727hg17UCSC Ensembl
Outerchr16:32606661..32607601hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38941
hg19941
hg18941
hg17941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19144
Known Genes
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)nssv24325
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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