A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24625



Internal ID15828425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14737295..14746476hg38UCSC Ensembl
Outerchr18:14736668..14748500hg38UCSC Ensembl
Innerchr18:14737294..14746475hg19UCSC Ensembl
Outerchr18:14736667..14748499hg19UCSC Ensembl
Innerchr18:14727294..14736475hg18UCSC Ensembl
Outerchr18:14726667..14738499hg18UCSC Ensembl
Innerchr18:14727294..14736475hg17UCSC Ensembl
Outerchr18:14726667..14738499hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3811833
hg1911833
hg1811833
hg1711833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9617
Supporting Variants
SamplesNA10839
Known GenesANKRD30B
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)nssv24625
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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