A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24941



Internal ID15486580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:857524..859439hg38UCSC Ensembl
Outerchr16:856661..867235hg38UCSC Ensembl
Innerchr16:907524..909439hg19UCSC Ensembl
Outerchr16:906661..917235hg19UCSC Ensembl
Innerchr16:847525..849440hg18UCSC Ensembl
Outerchr16:846662..857236hg18UCSC Ensembl
Innerchr16:847525..849440hg17UCSC Ensembl
Outerchr16:846662..857236hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810575
hg1910575
hg1810575
hg1710575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9326
Supporting Variants
SamplesNA18504
Known GenesLMF1
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)nssv24941
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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