A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19605



Internal ID15488302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131957313..131959164hg38UCSC Ensembl
Outerchr10:131956885..131959854hg38UCSC Ensembl
Innerchr10:133770817..133772668hg19UCSC Ensembl
Outerchr10:133770389..133773358hg19UCSC Ensembl
Innerchr10:133620807..133622658hg18UCSC Ensembl
Outerchr10:133620379..133623348hg18UCSC Ensembl
Innerchr10:133620807..133622658hg17UCSC Ensembl
Outerchr10:133620379..133623348hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382970
hg192970
hg182970
hg172970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8744
Supporting Variants
SamplesNA18537
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)nssv19605
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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