A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21584



Internal ID15834313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7052517..7097309hg38UCSC Ensembl
Outerchr10:7051040..7098102hg38UCSC Ensembl
Innerchr10:7094479..7139271hg19UCSC Ensembl
Outerchr10:7093002..7140064hg19UCSC Ensembl
Innerchr10:7134485..7179277hg18UCSC Ensembl
Outerchr10:7133008..7180070hg18UCSC Ensembl
Innerchr10:7134485..7179277hg17UCSC Ensembl
Outerchr10:7133008..7180070hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3847063
hg1947063
hg1847063
hg1747063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8603
Supporting Variants
SamplesNA18517
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)nssv21584
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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