A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv29243



Internal ID15841339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165578840..165604057hg38UCSC Ensembl
Outerchr3:165565820..165605563hg38UCSC Ensembl
Innerchr3:165296628..165321845hg19UCSC Ensembl
Outerchr3:165283608..165323351hg19UCSC Ensembl
Innerchr3:166779322..166804539hg18UCSC Ensembl
Outerchr3:166766302..166806045hg18UCSC Ensembl
Innerchr3:166779330..166804547hg17UCSC Ensembl
Outerchr3:166766310..166806053hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839744
hg1939744
hg1839744
hg1739744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10355
Supporting Variants
SamplesNA19007
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)nssv29243
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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