A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255



Internal ID15840760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153787278..153799313hg38UCSC Ensembl
Outerchr7:153786819..153799782hg38UCSC Ensembl
Innerchr7:153484363..153496398hg19UCSC Ensembl
Outerchr7:153483904..153496867hg19UCSC Ensembl
Innerchr7:153115296..153127331hg18UCSC Ensembl
Outerchr7:153114837..153127800hg18UCSC Ensembl
Innerchr7:152922011..152934046hg17UCSC Ensembl
Outerchr7:152921552..152934515hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3812964
hg1912964
hg1812964
hg1712964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8237
Supporting Variants
SamplesNA18980
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)nssv16255
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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