A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10528



Internal ID15845491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:106268396..106275220hg38UCSC Ensembl
Outerchr1:106811018..106817842hg19UCSC Ensembl
Outerchr1:106612541..106619365hg18UCSC Ensembl
Outerchr1:106523060..106529884hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg386825
hg196825
hg186825
hg176825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082
SamplesNA18502
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)nsv10528
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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