A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18385



Internal ID15840625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46830153..46868354hg38UCSC Ensembl
Outerchr10:46828584..46868427hg38UCSC Ensembl
Innerchr10:46684107..46719450hg19UCSC Ensembl
Outerchr10:46684034..46721006hg19UCSC Ensembl
Innerchr10:46104113..46139456hg18UCSC Ensembl
Outerchr10:46104040..46141012hg18UCSC Ensembl
Innerchr10:46104113..46139456hg17UCSC Ensembl
Outerchr10:46104040..46141012hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3839844
hg1936973
hg1836973
hg1736973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18980
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)nssv18385
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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