A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14777



Internal ID15489600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87466..91553hg38UCSC Ensembl
Outerchr1:86778..100645hg38UCSC Ensembl
Innerchr1:87466..91553hg19UCSC Ensembl
Outerchr1:86778..100645hg19UCSC Ensembl
Innerchr1:77329..81416hg18UCSC Ensembl
Outerchr1:76641..90508hg18UCSC Ensembl
Innerchr1:77329..81416hg17UCSC Ensembl
Outerchr1:76641..90508hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3813868
hg1913868
hg1813868
hg1713868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7879
Supporting Variants
SamplesNA18563
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)nssv14777
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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