A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21190



Internal ID15831954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14558105..14599686hg38UCSC Ensembl
Outerchr18:14557187..14600082hg38UCSC Ensembl
Innerchr18:14558104..14599685hg19UCSC Ensembl
Outerchr18:14557186..14600081hg19UCSC Ensembl
Innerchr18:14548104..14589685hg18UCSC Ensembl
Outerchr18:14547186..14590081hg18UCSC Ensembl
Innerchr18:14548104..14589685hg17UCSC Ensembl
Outerchr18:14547186..14590081hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3842896
hg1942896
hg1842896
hg1742896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9615
Supporting Variants
SamplesNA12802
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)nssv21190
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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