A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15258



Internal ID15489976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:60783..62747hg38UCSC Ensembl
Outerchr7:59936..63541hg38UCSC Ensembl
Innerchr7:60783..62747hg19UCSC Ensembl
Outerchr7:59936..63541hg19UCSC Ensembl
Innerchr7:155866..157830hg18UCSC Ensembl
Outerchr7:155019..158624hg18UCSC Ensembl
Innerchr7:155866..157830hg17UCSC Ensembl
Outerchr7:155019..158624hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383606
hg193606
hg183606
hg173606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8023
Supporting Variants
SamplesNA18564
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)nssv15258
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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