A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24094



Internal ID15483151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32356402..32441008hg38UCSC Ensembl
Outerchr16:32356309..32441356hg38UCSC Ensembl
Innerchr16:32367723..32452329hg19UCSC Ensembl
Outerchr16:32367630..32452677hg19UCSC Ensembl
Innerchr16:32275224..32359830hg18UCSC Ensembl
Outerchr16:32275131..32360178hg18UCSC Ensembl
Innerchr16:32275224..32359830hg17UCSC Ensembl
Outerchr16:32275131..32360178hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3885048
hg1985048
hg1885048
hg1785048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA11830
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)nssv24094
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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