A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22287



Internal ID15841893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123459617..123460862hg38UCSC Ensembl
Outerchr10:123458857..123461854hg38UCSC Ensembl
Innerchr10:125219133..125220378hg19UCSC Ensembl
Outerchr10:125218373..125221370hg19UCSC Ensembl
Innerchr10:125209123..125210368hg18UCSC Ensembl
Outerchr10:125208363..125211360hg18UCSC Ensembl
Innerchr10:125209123..125210368hg17UCSC Ensembl
Outerchr10:125208363..125211360hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382998
hg192998
hg182998
hg172998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8734
Supporting Variants
SamplesNA19132
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)nssv22287
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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