A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23725



Internal ID15491244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55691707..55699032hg38UCSC Ensembl
Outerchr11:55685516..55701112hg38UCSC Ensembl
Innerchr11:55459183..55466508hg19UCSC Ensembl
Outerchr11:55452992..55468588hg19UCSC Ensembl
Innerchr11:55215759..55223084hg18UCSC Ensembl
Outerchr11:55209568..55225164hg18UCSC Ensembl
Innerchr11:55215759..55223084hg17UCSC Ensembl
Outerchr11:55209568..55225164hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3815597
hg1915597
hg1815597
hg1715597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8827
Supporting Variants
SamplesNA18860
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)nssv23725
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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