A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466



Internal ID15483016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181405829..181461285hg38UCSC Ensembl
Outerchr5:181405802..181462876hg38UCSC Ensembl
Innerchr5:180832830..180888286hg19UCSC Ensembl
Outerchr5:180832803..180889877hg19UCSC Ensembl
Innerchr5:180765436..180820892hg18UCSC Ensembl
Outerchr5:180765409..180822483hg18UCSC Ensembl
Innerchr5:180765436..180820892hg17UCSC Ensembl
Outerchr5:180765409..180822483hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857075
hg1957075
hg1857075
hg1757075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10793
Supporting Variants
SamplesNA10863
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)nssv14466
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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