A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22862



Internal ID15830800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20921745..20926083hg38UCSC Ensembl
Outerchr15:20920690..20926678hg38UCSC Ensembl
Innerchr15:21127074..21131412hg19UCSC Ensembl
Outerchr15:21126019..21132007hg19UCSC Ensembl
Innerchr15:19391731..19396071hg18UCSC Ensembl
Outerchr15:19390673..19396666hg18UCSC Ensembl
Innerchr15:19391731..19396071hg17UCSC Ensembl
Outerchr15:19390673..19396666hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385989
hg195989
hg185994
hg175994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
Known GenesNF1P2
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)nssv22862
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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