A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23510



Internal ID15827416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14737295..14743078hg38UCSC Ensembl
Outerchr18:14736668..14744333hg38UCSC Ensembl
Innerchr18:14737294..14743077hg19UCSC Ensembl
Outerchr18:14736667..14744332hg19UCSC Ensembl
Innerchr18:14727294..14733077hg18UCSC Ensembl
Outerchr18:14726667..14734332hg18UCSC Ensembl
Innerchr18:14727294..14733077hg17UCSC Ensembl
Outerchr18:14726667..14734332hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387666
hg197666
hg187666
hg177666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9617
Supporting Variants
SamplesNA07029
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)nssv23510
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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