A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19277



Internal ID15489304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45896153..45901651hg38UCSC Ensembl
Outerchr10:45895541..45902101hg38UCSC Ensembl
Innerchr10:46391601..46397099hg19UCSC Ensembl
Outerchr10:46390989..46397549hg19UCSC Ensembl
Innerchr10:45711607..45717105hg18UCSC Ensembl
Outerchr10:45710995..45717555hg18UCSC Ensembl
Innerchr10:45711607..45717105hg17UCSC Ensembl
Outerchr10:45710995..45717555hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386561
hg196561
hg186561
hg176561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8631
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)nssv19277
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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