A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22901



Internal ID15490081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:30296237..30315976hg38UCSC Ensembl
Outerchr16:30296186..30317028hg38UCSC Ensembl
Innerchr16:30307558..30327297hg19UCSC Ensembl
Outerchr16:30307507..30328349hg19UCSC Ensembl
Innerchr16:30215059..30234798hg18UCSC Ensembl
Outerchr16:30215008..30235850hg18UCSC Ensembl
Innerchr16:30215059..30234798hg17UCSC Ensembl
Outerchr16:30215008..30235850hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820843
hg1920843
hg1820843
hg1720843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9433
Supporting Variants
SamplesNA18564
Known GenesLOC440354, LOC595101
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)nssv22901
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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